← Product Code [KTI](/productcode/KTI) · K261274 # EchoTip Ultra® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes; EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes (K261274) _Cook Ireland, Ltd. · KTI · Jul 24, 2026 · Ear, Nose, Throat · SESE_ **Canonical URL:** https://fda-staging.innolitics.com/device/K261274 ## Device Facts - **Applicant:** Cook Ireland, Ltd. - **Product Code:** [KTI](/productcode/KTI.md) - **Decision Date:** Jul 24, 2026 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 874.4680 - **Device Class:** Class 2 - **Review Panel:** Ear, Nose, Throat ## Indications for Use EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes: This device is used to sample targeted submucosal and extramural lesions within or adjacent to the tracheobronchial tree through the accessory channel of an ultrasound endoscope for fine needle aspiration (FNA). EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes: This device is used with an ultrasound endoscope for fine needle biopsy (FNB) of submucosal and extramural lesions within or adjacent to the tracheobronchial tree. ## Device Story Endoscopic ultrasound needles (22G, 25G) for sampling submucosal/extramural lesions in/near tracheobronchial tree; used with Fujifilm EBUS scopes. Device includes needle assembly, syringe, and accessory channel adapter. Adapter provides Luer fitting for Fujifilm scope compatibility; sheath length and needle extension adjustable via handle. Procedure: device inserted into scope channel; needle punctures target; vacuum applied via syringe stopcock; handle moved in small increments to collect sample; needle retracted into sheath for removal. Used in clinical settings by professionals. Benefits: enables ultrasound-guided tissue sampling for diagnostic purposes. ## Clinical Evidence No clinical data. Substantial equivalence supported by bench testing only. Simulated use testing confirmed that the modified adapter maintains performance characteristics consistent with the reference device (K210476). ## Technological Characteristics Needle cannula: 304 stainless steel; Wire: Nitinol. Manual operation. Single-use. Sterilization: Ethylene Oxide (EO). Includes accessory channel adapter for Fujifilm scope Luer compatibility. Sheath/needle adjustment via handle with safety ring, thumbscrews, and graduation markers. Compatible with minimum 2.0 mm endoscope channel. ## Regulatory Identification A bronchoscope (flexible or rigid) and accessories is a tubular endoscopic device with any of a group of accessory devices which attach to the bronchoscope and is intended to examine or treat the larynx and tracheobronchial tree. It is typically used with a fiberoptic light source and carrier to provide illumination. The device is made of materials such as stainless steel or flexible plastic. This generic type of device includes the rigid ventilating bronchoscope, rigid nonventilating bronchoscope, nonrigid bronchoscope, laryngeal-bronchial telescope, flexible foreign body claw, bronchoscope tubing, flexible biopsy forceps, rigid biopsy curette, flexible biopsy brush, rigid biopsy forceps, flexible biopsy curette, and rigid bronchoscope aspirating tube, but excludes the fiberoptic light source and carrier. ## Predicate Devices - ViziShot 2 FLEX ([K193517](/device/K193517.md)) ## Reference Devices - EchoTip Ultra® Endobronchial High-Definition Ultrasound Needle for Olympus Scopes ([K210476](/device/K210476.md)) - EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Olympus Scopes ([K210476](/device/K210476.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0} **U.S. FOOD & DRUG** ADMINISTRATION July 24, 2026 Cook Ireland, Ltd. Caoimhe Murphy Official Correspondent O'Halloran Rd. National Technology Park, Plassey Limerick, N/A V94 N8X2 Ireland Re: K261274 Trade/Device Name: EchoTip Ultra® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes; EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes Regulation Number: 21 CFR 874.4680 Regulation Name: Bronchoscope (flexible or rigid) and accessories Regulatory Class: Class II Product Code: KTI Dated: April 17, 2026 Received: April 17, 2026 Dear Caoimhe Murphy: We have reviewed your section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (the Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database available at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of {1} K261274 - Caoimhe Murphy Page 2 Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. Additional information about changes that may require a new premarket notification are provided in the FDA guidance documents entitled "Deciding When to Submit a 510(k) for a Change to an Existing Device" (https://www.fda.gov/media/99812/download) and "Deciding When to Submit a 510(k) for a Software Change to an Existing Device" (https://www.fda.gov/media/99785/download). Your device is also subject to, among other requirements, the Quality Management System Regulation (QMSR) (21 CFR Part 820), which includes, but is not limited to, ISO 13485 clause 7.3 (Design controls), ISO 13485 clause 8.3 (Nonconforming product), ISO 13485 clause 8.5.2 (Corrective action), and ISO 13485 clause 8.5.3 (Preventative action). Please note that regardless of whether a change requires premarket review, the QMSR requires device manufacturers to review and approve changes to device design and production (ISO 13485 clause 7.3 and ISO 13485 clause 7.5) and document changes and approvals in the Medical Device File (ISO 13485 clause 4.2.3). Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR Part 803) for devices or postmarketing safety reporting (21 CFR Part 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reporting-combination-products); good manufacturing practice requirements as set forth in the Quality Management System Regulation (QMSR) (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR Part 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR Parts 1000-1050. All medical devices, including Class I and unclassified devices and combination product device constituent parts are required to be in compliance with the final Unique Device Identification System rule ("UDI Rule"). The UDI Rule requires, among other things, that a device bear a unique device identifier (UDI) on its label and package (21 CFR 801.20(a)) unless an exception or alternative applies (21 CFR 801.20(b)) and that the dates on the device label be formatted in accordance with 21 CFR 801.18. The UDI Rule (21 CFR 830.300(a) and 830.320(b)) also requires that certain information be submitted to the Global Unique Device Identification Database (GUDID) (21 CFR Part 830 Subpart E). For additional information on these requirements, please see the UDI System webpage at https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/unique-device-identification-system-udi-system. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-devices/medical-device-safety/medical-device-reporting-mdr-how-report-medical-device-problems. For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn {2} K261274 - Caoimhe Murphy Page 3 (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100). Sincerely, John S. Bender -S for Ethan Nyberg, Ph.D. Assistant Director DHT1C: Division of Anesthesia, Respiratory, and Sleep Devices OHT1: Office of Ophthalmic, Anesthesia, Respiratory, ENT, and Dental Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health Enclosure {3} DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration # Indications for Use Form Approved: OMB No. 0910-0120 Expiration Date: 07/31/2026 See PRA Statement below. 510(k) Number (if known) K261274 Device Name EchoTip Ultra® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes Indications for Use (Describe) EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes: This device is used to sample targeted submucosal and extramural lesions within or adjacent to the tracheobronchial tree through the accessory channel of an ultrasound endoscope for fine needle aspiration (FNA). EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes: This device is used with an ultrasound endoscope for fine needle biopsy (FNB) of submucosal and extramural lesions within or adjacent to the tracheobronchial tree. Type of Use (Select one or both, as applicable) ☑ Prescription Use (Part 21 CFR 801 Subpart D) ☐ Over-The-Counter Use (21 CFR 801 Subpart C) # CONTINUE ON A SEPARATE PAGE IF NEEDED. This section applies only to requirements of the Paperwork Reduction Act of 1995. # *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.* The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." FORM FDA 3881 (8/23) Page 1 of 1 PSC Publishing Services (301) 443-6740 EF {4} EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes 510(K) Summary K261274 # **510(k) Summary - K261274** **EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes** **EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes** **21 CFR §876.1075** **Date Prepared: 24 July 2026** # **Submitted By:** Submission: Traditional 510(k) Premarket Notification- K261274 Applicant: Cook Ireland Ltd Applicant Address: O'Halloran Road National Technology Park Plassey Limerick V94 N8X2, Ireland Contact: Caoimhe Murphy Email: Caoimhe.Murphy@CookMedical.com Contact Phone Number: +35361334440 # **Device Information:** Trade Name: EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes **Device Common Name:** Bronchoscope (flexible or rigid) and Accessories. **Classification Regulation:** 21 CFR 874.4680 **Product Code:** KTI **Device Classification:** Class II # **Predicate Device:** ViziShot 2 FLEX (K193517, Olympus Surgical Technologies America, Gyrus ACMI, Inc.) # **Reference Device:** EchoTip Ultra® Endobronchial High-Definition Ultrasound Needle for Olympus Scopes and the EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Olympus Scopes (K210476, Cook Ireland Ltd). # **Device Description:** The EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes and the EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes are endoscopic ultrasound needles, available in two different needle sizes (22 and 25 gauge), and contain the following components: Page 1 of 7 {5} EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes 510(K) Summary K261274 a needle assembly, syringe and an accessory channel adapter for use with the Fujifilm endobronchial ultrasound (EBUS) scope. Fujifilm EBUS scopes do not have a Luer fitting to allow needle attachment directly to the accessory channel port. The EchoTip Ultra and EchoTip Procore Endobronchial HD Ultrasound Needle for Fujifilm Scopes are supplied with an accessory channel adapter to function as a Luer fitting, to which the needle can be connected. The device is inserted into the scope accessory channel and attached when the fittings meet. The sheath length can be adjusted depending on the length of the EBUS scope using the sliding sheath adjuster. The needle length extension can be adjusted as required. The device is used to puncture the target site to obtain a sample. If using a standard vacuum syringe technique, the stylet is then removed, and the syringe is attached to the Luer fitting on the needle handle. Turning the syringe stopcock to the “open” position allows negative pressure to aspirate the sample. The handle is gently moved in small increments back and forth within the target site to obtain a sample. If using the syringe, the stopcock is returned to the “closed” position. The needle is retracted into the sheath and the device is disconnected from the scope accessory channel. Upon completion of the procedure the adapter is removed from the accessory channel port. The Adapter Component is the only modification to the reference device, consisting of a colour change and a dimensional modification to the ‘Adapter Base’ permitting compatibility to the Fujifilm Scope. ### **Indications for Use:** #### *EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes:* This device is used to sample targeted submucosal and extramural lesions within or adjacent to the tracheobronchial tree through the accessory channel of an ultrasound endoscope for fine needle aspiration (FNA). #### *EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes:* This device is used with an ultrasound endoscope for fine needle biopsy (FNB) of submucosal and extramural lesions within or adjacent to the tracheobronchial tree. ### **Technological Comparison:** Both the subject device and the predicate, ViziShot 2 FLEX, has been designed to be used with ultrasound endoscopes, indicated for ultrasound guided fine needle aspiration (FNA) and fine needle biopsy (FNB) of submucosal and extramural lesions of the tracheobronchial tree. There are technological similarities and differences between the subject device, EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes and the EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Page 2 of 7 {6} EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes 510(K) Summary K261274 Scopes, and the predicate, ViziShot 2 FLEX. Refer to Table 1 for Comparison of Technological Characteristics. The subject device has the same technological characteristics and design as the reference device, EchoTip Ultra® Endobronchial High-Definition Ultrasound Needle for Olympus Scopes and the EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Olympus Scopes, cleared under K210476 on May 20th, 2021. The Adapter Component is the only design modification to the reference device, which includes a colour change and a dimensional modification to the ‘Adapter Base’ permitting compatibility to the Fujifilm Scope. Refer to Table 1 for Comparison of Technological Characteristics: | Parameter | Subject Device: | Predicate Device: | Reference Device | Comparison | | --- | --- | --- | --- | --- | | Device Name | EchoTip Ultra® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes / EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes | ViziShot 2 FLEX | EchoTip Ultra® Endobronchial High- Definition Ultrasound Needle EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Olympus Scopes | | | 510(k) Number | K261274 | K193517 | K210476 | | Page 3 of 7 {7} EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes 510(K) Summary K261274 | Parameter | Subject Device: | Predicate Device: | Reference Device | Comparison | | --- | --- | --- | --- | --- | | **Indications for Use** | *EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes:* This device is used to sample targeted submucosal and extramural lesions within or adjacent to the tracheobronchial tree through the accessory channel of an ultrasound endoscope for fine needle aspiration (FNA). *EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes:* This device is used with an ultrasound endoscope for fine needle biopsy (FNB) of submucosal and extramural lesions within or adjacent to the tracheobronchial tree. | The ViziShot 2 FLEX has been designed to be used with ultrasound endoscopes for ultrasound guided fine needle aspiration (FNA) and fine needle biopsy (FNB) of submucosal and extramural lesions of the Tracheobronchial tree. Do not use this device for any purpose other than its intended use. | *EchoTip Ultra® Endobronchial HD Ultrasound Needle for Olympus Scopes:* This device is used to sample targeted submucosal and extramural lesions within or adjacent to the tracheobronchial tree or gastrointestinal tract through the accessory channel of an ultrasound endoscope for Fine Needle Aspiration (FNA) *EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Olympus Scopes:* This device is used with an ultrasound endoscope for fine needle biopsy, (FNB), of submucosal and extramural lesions within or adjacent to the tracheobronchial tree or gastrointestinal tract. | Similar to the Predicate device. | | **FDA Classification Code** | KTI | KTI | FCG | Identical to the predicate | | **Anatomical Sites** | Tracheobronchial tree. | Tracheobronchial tree. | Tracheobronchial tree and gastrointestinal tract | Identical to the predicate | | **Needle Cannula Material** | 304 Stainless Steel | Unknown | 304 Stainless Steel | Identical to the reference device, | Page 4 of 7 {8} EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes 510(K) Summary K261274 | Parameter | Subject Device: | Predicate Device: | Reference Device | Comparison | | --- | --- | --- | --- | --- | | **Wire Material** | Nitinol | Unknown | Nitinol | K193517 lists combined patient-contacting materials only (Stainless Steel, PTFE, PEBAX, Nitinol) | | **Needle Gauge** | 22G, 25G | 19G | 22G, 25G | Identical to the reference device | | **Stylet Shape Upon Removal** | Straight | Unknown | Straight | Identical to the reference device | | **Method for Sheath / Needle Adjustment** | Handle with a safety ring and sheath adjuster including thumbscrews that enable needle and sheath adjustment. Graduation markers indicate extension. | Lever-lock handle advancement; no sheath adjustment reported | Handle with a safety ring and sheath adjuster including thumbscrews that enable needle and sheath adjustment. Graduation markers indicate extension. | Identical to the reference device | | **Minimum Compatible Endoscope Channel Size** | 2.0 mm | 2.2 mm | 2.0 mm | Identical to the reference device | | **Supplied with Syringe (with Stopcock)** | Yes | Yes | Yes | Identical | | **Mechanism / Principle of Operation** | Manual | Manual | Manual | Identical | | **Device Usage** | For Professional Use | For Professional Use | For Professional Use | Identical | | **Single Use or Reusable** | Single Use | Single Use | Single Use | Identical | Page 5 of 7 {9} EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes 510(K) Summary K261274 | Parameter | Subject Device: | Predicate Device: | Reference Device | Comparison | | --- | --- | --- | --- | --- | | **Method of connection to compatible Scope** | The EchoTip Ultra and EchoTip Procore Endobronchial HD Ultrasound Needle for Fujifilm Scopes are supplied with an accessory channel adapter to function as a Luer fitting, to which the needle can be connected. | The handle is then affixed to the channel port of the endoscope via a lever mechanism that locks onto the Adapter Biopsy Valve. | The EchoTip Ultra and EchoTip Procore Endobronchial HD Ultrasound Needle for Olympus Scopes are supplied with an accessory channel adapter to function as a Luer fitting, to which the needle can be connected. | Identical to the reference device | | **Method of Sterilization** | EO | EO | EO | Identical | | **Accessory channel adapter Base color** | Black | Unknown | Grey | Different | | **Scope Compatibility** | Fujifilm Scope | Ultrasound Endoscope (Brand not reported) | Olympus Scope | Different | | **Accessory channel Adapter Base Component** | Present | Unknown | Present | The accessory channel adapter base component is Dimensionally Different to the reference device. | # **Performance Data:** The subject device, EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes and the EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes, is identical to the reference device, EchoTip Ultra® Endobronchial High-Definition Ultrasound Needle for Olympus Scopes and the EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Olympus Scopes (K210476, Cook Ireland Ltd) in all design and technological characteristics except for the Adapter Component, which is the only design modification to the reference device. Bench testing was conducted on the modified devices to ensure that the devices meet pre-determined acceptance criteria, and to confirm the performance characteristics of the devices. The simulated use testing performed utilised a well-established test method applied to the reference devices cleared under K210476. Page 6 of 7 {10} EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes 510(K) Summary K261274 ## Conclusion All device non-clinical bench test results are acceptable. Data demonstrates that the EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes and the EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes with the modified adapter meets the design specifications and the pre-defined acceptance criteria. Cook Ireland Ltd. has demonstrated that the subject device, EchoTip Ultra® Endobronchial HD Ultrasound Needle for Fujifilm Scopes and the EchoTip ProCore® Endobronchial HD Ultrasound Biopsy Needle for Fujifilm Scopes with the modified adapter is substantially equivalent to the predicate devices and presents no new questions of safety or effectiveness. Page 7 of 7 --- **Source:** [https://fda-staging.innolitics.com/device/K261274](https://fda-staging.innolitics.com/device/K261274) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com