← Product Code [BZD](/productcode/BZD) · K261262 # Altis Full Face Mask (K261262) _Respironics, Inc. · BZD · Sep 25, 2026 · Anesthesiology · SESE_ **Canonical URL:** https://fda-staging.innolitics.com/device/K261262 ## Device Facts - **Applicant:** Respironics, Inc. - **Product Code:** [BZD](/productcode/BZD.md) - **Decision Date:** Sep 25, 2026 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 868.5905 - **Device Class:** Class 2 - **Review Panel:** Anesthesiology - **Attributes:** Therapeutic ## Indications for Use The Altis Full Face Mask is intended to provide an interface for the application of non-invasive positive airway pressure (PAP) therapy. The mask is intended for single-patient reuse in the home environment and healthcare facilities and/or hospital environments. The mask is to be used by adult patients aged 22 years and older weighing more than 66lb (30kg) for whom non-invasive PAP therapy has been prescribed. The device is not intended for critical care patients. ## Device Story Altis Full Face Mask; over-the-nose/mouth interface for non-invasive PAP therapy. Components: cushion (polycarbonate faceplate, silicone seal), frame, exhalation elbow, headgear, magnetic clips. Connects to standard ISO 5356-1 22mm hoses. Used in home and hospital settings; operated by patients or healthcare providers. Delivers pressurized air to airways. Bench-tested for flow, resistance, CO2 rebreathing, and biocompatibility. No clinical data required. ## Clinical Evidence No clinical data. Safety and effectiveness demonstrated via non-clinical bench testing, including ISO 17510:2015 performance testing (exhaust flow, resistance, CO2 rebreathing, anti-asphyxia valve, noise), biocompatibility (ISO 10993, ISO 18562), and cleaning validation. ## Technological Characteristics Materials: polycarbonate, silicone, polypropylene, woven/laminate fabrics, magnets. Interface: full face mask with exhalation elbow. Connectivity: ISO 5356-1 22mm conical hose connection. Pressure range: 4-40 cm H2O. Non-sterile. Biocompatibility per ISO 10993 and ISO 18562. Performance per ISO 17510:2015. ## Regulatory Identification A noncontinuous ventilator (intermittent positive pressure breathing-IPPB) is a device intended to deliver intermittently an aerosol to a patient's lungs or to assist a patient's breathing. ## Predicate Devices - Resmed AirFit F20 Mask System; AirFit F20 NM Mask System ([K242547](/device/K242547.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} FDA U.S. FOOD & DRUG ADMINISTRATION September 25, 2026 Respironics, Inc. Viralyne Lipps Principal Regulatory Affairs Specialist 1001 Murry Ridge Ln. Murrysville, Pennsylvania 15668 Re: K261262 Trade/Device Name: Altis Full Face Mask Regulation Number: 21 CFR 868.5905 Regulation Name: Noncontinuous Ventilator (IPPB) Regulatory Class: Class II Product Code: BZD Dated: August 28, 2026 Received: August 28, 2026 Dear Viralyne Lipps: 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 Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. Before making any change significantly affecting the safety or effectiveness of the device, you must submit a new premarket notification in accordance with 21 CFR 807.81. Additional information about changes that may require a new premarket notification are provided in the FDA guidance documents entitled "Deciding U.S. Food & Drug Administration 10903 New Hampshire Avenue Silver Spring, MD 20993 www.fda.gov {1} K261262 - Viralyne Lipps Page 2 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 (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- {2} K261262 - Viralyne Lipps Page 3 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, Binoy J. Mathews -S Digitally signed by Binoy J. Mathews -S Date: 2026.09.25 12:02:32 -04'00' For James Lee, PhD Division 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} | Indications for Use | | | | --- | --- | --- | | Please type in the marketing application/submission number, if it is known. This textbox will be left blank for original applications/submissions. | K261262 | ? | | Please provide the device trade name(s). | | ? | | Altis Full Face Mask | | | | Please provide your Indications for Use below. | | ? | | The Altis Full Face Mask is intended to provide an interface for the application of non-invasive positive airway pressure (PAP) therapy. The mask is intended for single-patient reuse in the home environment and healthcare facilities and/or hospital environments. The mask is to be used by adult patients aged 22 years and older weighing more than 66lb (30kg) for whom non-invasive PAP therapy has been prescribed. The device is not intended for critical care patients. | | | | Please select the types of uses (select one or both, as applicable). | ☑ Prescription Use (21 CFR 801 Subpart D) ☐ Over-The-Counter Use (21 CFR 801 Subpart C) | ? | | Please select the age group(s) for which the device(s) is to be used. | ☐ Neonates/Newborns (Birth to < 29 days old) ☐ Infants (29 days old to < 2 years old) ☐ Children (2 years old to < 12 years old) ☐ Adolescents (12 years old to < 22 years old) ☑ Adults (22 years old and greater) | ? | {4} PHILIPS Altis Full Face Mask Traditional 510(k) K261262 ### 510(k) Summary [As required by 21 CFR 807.92(c)] Date Prepared: September 24, 2026 ### I. Submitter Company Name/Owner: Respironics, Inc. 1001 Murry Ridge Lane Murrysville, PA 15668, USA Official Contact: Viralyne Lipps Principal Regulatory Affairs Specialist ### II. Device Device Trade Name: Altis Full Face Mask Device Common Name: Full Face Mask Regulation Number: 21 CFR 868.5905 Classification Name: Noncontinuous ventilator (IPPB) Product Code: BZD Device Classification: Class II ### III. Predicate Device Predicate Device: Resmed AirFit F20 Mask System; AirFit F20 NM Mask System (K242547) Regulation Number: 21 CFR 868.5905 Classification Name: Noncontinuous ventilator (IPPB) Product Code: BZD This predicate has not been the subject of a design-related recall. ### IV. Device Description The Altis Full Face Mask is an over-the-nose, full-face mask with the hose connection in the front. The mask covers both the nose and mouth, ensuring pressurized air is delivered directly into the patient's airways with the use of a positive airway pressure (PAP) therapy device; it is intended for single-patient reuse in the home and healthcare facilities and/or hospital environments. The mask consists of five main parts: a cushion (polycarbonate faceplate and bond ring with silicone seal), frame, exhalation elbow, headgear, and headgear clips. The elbow connects to standard ISO 5356-1 22 mm conical hoses. ### V. Indications For Use The Altis Full Face Mask is intended to provide an interface for the application of non-invasive positive airway pressure (PAP) therapy. The mask is intended for single-patient reuse in the home environment and healthcare facilities and/or hospital environments. The mask is to be used by adult patients aged 22 years and older weighing more than 66 lb (30 kg) for whom non-invasive PAP therapy has been prescribed. The device is not intended for critical care patients. Page 1 of 6 {5} PHILIPS Altis Full Face Mask Traditional 510(k) K261262 # VI. Comparison with Predicate Device | Design/Technological Characteristic | Subject Device Altis Full Face Mask | Predicate Device AirFit F20 and Air Fit NM Mask Systems (K242547) | Comments | | --- | --- | --- | --- | | Product Code | BZD | BZD | Identical | | Regulation Number | 21 CFR 868.5905 | 12 CFR 868.5905 | Identical | | Classification Name | Non-continuous ventilator | Non-continuous ventilator | Identical | | Regulatory Class | Class II | Class II | Identical | | Classification Panel | Anesthesiology | Anesthesiology | Identical | | Indications for Use / Intended Use | The Altis Full Face Mask is intended to provide an interface for the application of non-invasive positive airway pressure (PAP) therapy. The mask is intended for single-patient reuse in the home environment and healthcare facilities and/or hospital environments. The mask is to be used by adult patients aged 22 years and older weighing more than 66 lb (30 kg) for whom non-invasive PAP therapy has been prescribed . The device is not intended for critical care patients. | The AirFit F20 masks have two product variants: - The AirFit F20 variants are intended for single-patient reuse in the home environment - The AirFit F20 SLM (Sleep Lab Masks) variants are intended for multi-patient reuse in the hospital/institutional environment.These masks are intended for patients weighing more than 66lb (30kg), who have been prescribed non-invasive CPAP or bi-level positive airway pressure (PAP) therapy. The Sleep Lab Masks are the only variants that are validated and intended for multi-patient reprocessing and must be reprocessed if reused between patients | Equivalent | | Availability | Prescription use only | Prescription use only | Identical | | Patient Population | Adult patients weighing more than 66 lb (30 kg) | Patients weighing more than 66 lb (30 kg) | Equivalent | | Anatomical Sites | Nose and mouth | Nose and mouth | Identical | | Operating Environment | Home or healthcare facilities and/or hospitals | Home or health institution | Equivalent | | Operating and Storage Temperature Range | Operating: 5 °C to 40 °C Storage: -20 °C to +60 °C | Operating: 5 °C to 40 °C Storage: -20 °C to +60 °C | Identical | | Patient Circuit Connection | ISO 5356-1 (22 mm) | ISO 5356-1 (22 mm) | Identical | | Sizes | Cushion available in four sizes Headgear available in two sizes Frame available in one size | Cushion available in three sizes Headgear available in three sizes Frame available in one size | Equivalent | | Exhalation Vent | Multi-hole vent array | Multi-hole vent | Equivalent | | Sterile State as Provided | Non-sterile | Non-sterile | Identical | Page 2 of 6 {6} PHILIPS Altis Full Face Mask Traditional 510(k) K261262 | Design/Technological Characteristic | Subject Device Altis Full Face Mask | | Predicate Device AirFit F20 and Air Fit NM Mask Systems (K242547) | | Comments | | --- | --- | --- | --- | --- | --- | | Pressure Range | 4 to 40 cm H_{2}O | | 3 to 40 cm H_{2}O | | Equivalent | | Mask Exhaust Flow (nominal) | Pressure (cmH_{2}O) | SLPM | Pressure (cmH_{2}O) | SLPM | Equivalent Disclosed per ISO 17510:2015 Annex B | | | 4 | 16 | 3 | 19 | | | | 13 | 32 | 20 | 54 | | | | 22 | 44 | 40 | 82 | | | | 31 | 55 | | | | | | 40 | 64 | | | | | Resistance to Flow (pressure drop) | @50l/min | @100l/min | @50l/min | @100l/min | Equivalent Disclosed per ISO 17510:2015 Annex C | | | 0.2 cmH_{2}O | 0.9 cmH_{2}O | 0.2 cmH_{2}O | 0.6 cmH_{2}O | | | Anti-Asphyxia Valve Operation | Open to atmosphere | Closed to atmosphere | Open to atmosphere | Closed to atmosphere | Equivalent (