← Product Code [LZA](/productcode/LZA) · K981333 # NITRILON CORRECT-TOUCH (K981333) _Biopro (M) Sdn Bhd · LZA · Jun 22, 1998 · General Hospital · SESE_ **Canonical URL:** https://fda-staging.innolitics.com/device/K981333 ## Device Facts - **Applicant:** Biopro (M) Sdn Bhd - **Product Code:** [LZA](/productcode/LZA.md) - **Decision Date:** Jun 22, 1998 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 880.6250 - **Device Class:** Class 1 - **Review Panel:** General Hospital ## Indications for Use A medical glove is worn on the hand of health care personnel to prevent contamination between health care personnel and the patient. ## Device Story Nitrilon™ Correct-Touch® Nitrile Powder-Free Examination Gloves are disposable medical gloves designed for use by healthcare personnel. The device acts as a physical barrier to prevent cross-contamination between the clinician and the patient during medical examinations or procedures. The gloves are worn on the hands of the user. They are intended for over-the-counter use in clinical or point-of-care settings. The device provides a protective layer to reduce the risk of transmission of infectious agents or contaminants. ## Clinical Evidence No clinical data provided; bench testing only. ## Technological Characteristics Nitrile examination glove; powder-free; disposable; non-sterile; physical barrier design. ## Regulatory Identification A non-powdered patient examination glove is a disposable device intended for medical purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner. A non-powdered patient examination glove does not incorporate powder for purposes other than manufacturing. The final finished glove includes only residual powder from manufacturing. ## 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}------------------------------------------------ Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is an abstract symbol that resembles a stylized caduceus or a representation of human figures. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 JUN 2 2 1998 Biopro (M) Sdn. Bhd. ·C/O Mr. Mike Kyle President CT International 4349 Santa Fe Road San Luis Obispo, California 93401 K981333 Re : Nitrilon™ Correct-Touch® Nitrile Powder-Trade Name: Free Examination Gloves Regulatory Class: I Product Code: LZA Dated: April 13, 1998 Received: April 13, 1998 Dear Mr. Kyle: We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to 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 (Act). You may, therefore, market the device, subject to the general controls provisions The general controls provisions of the Act of the Act. include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may be subject to such additional controls. Existing major requlations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the Good Manufacturing Practice for Medical Devices: General (GMP) requlation (21 CFR Part 820) and that, through periodic GMP inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP requlation may result in requlatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of {1}------------------------------------------------ Page 2 - Mr. Kyle the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations. This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4692. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2040 or (301) 443-6597 or at its internet address "http://www.fda/gov/cdrh/dsmamain.html". Sincerely yours, Timothy A. Ulatowski Director Division of Dental, Infection Control, and General Hospital Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ CT INTERNATIONAL →→→→ かついんでは気になるという 1 11 0 0 2 0 0 1 ## Indications for Use Statement: 3.0 Applicant: CT International for Biopro (M) Sdn. Bhd. 510(k) Number (if known): K9 8 | 333 333 Examination Glove Device Name: Indications For Use: A medical glove is worn on the hand of A medical grow similar personnel to prevent contamination between health care personnel and the patient. (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)____________________________________________________________________________________________________ Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109) OR Over-The-Counter Use X (Optional Format 1-2-96) Qun S. Lin (Division Sign-Off) Division of Dental, Infection Control, and General Hospital Devic 510(k) Number --- **Source:** [https://fda-staging.innolitics.com/device/K981333](https://fda-staging.innolitics.com/device/K981333) **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