(39 days)
A powder-Free patient examination glove is a disposable device made of natural rubber latex that may bear a trace amount of glove powder and is intended to be worn on the examiner's hand or finger's for medical purposes to provide a barrier against potentially infectious materials and other contaminants.
Powder-Free Polymer-Coated Latex Examination Gloves
The provided text describes a 510(k) premarket notification for "Ever-More Powder-Free Polymer-Coated Latex Examination Gloves." This is a regulatory document affirming substantial equivalence to a predicate device, not a study reporting on the performance of a medical device against acceptance criteria in the manner of AI/ML or imaging diagnostics.
Therefore, none of the requested information regarding acceptance criteria, sample sizes, expert involvement, adjudication, MRMC studies, standalone performance, or training/ground truth establishment is present in the provided document.
The document details the regulatory classification of the device (Class I), its regulation number (880.6250), product code (LYY), and its intended use as a barrier against potentially infectious materials. It also confirms that the FDA has determined the device to be substantially equivalent to legally marketed predicate devices.
Summary of missing information:
- Table of acceptance criteria and reported device performance: Not available. This document is about regulatory clearance, not performance testing.
- Sample sizes used for the test set and data provenance: Not applicable. No test set described.
- Number of experts used to establish the ground truth for the test set and their qualifications: Not applicable. No ground truth establishment for a test set.
- Adjudication method for the test set: Not applicable. No test set adjudication.
- Multi-reader multi-case (MRMC) comparative effectiveness study: Not applicable. This is not an AI/ML or imaging diagnostic device.
- Standalone performance (algorithm only without human-in-the-loop performance): Not applicable. This is a physical glove, not an algorithm.
- Type of ground truth used: Not applicable.
- Sample size for the training set: Not applicable.
- How the ground truth for the training set was established: Not applicable.
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DEPARTMENT OF HEALTH & HUMAN SERVICES
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Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
V 2 9 2002
Mr. Chia Meng Cheng Deputy General Manager Ever-More Latex Products Sdn. Bhd. Lot 555, 6 3/4 Mile, Jalan Gangsa, Durian Tunggal. 76100 Melaka MALAYSIA
Re: K023523
Trade/Device Name: Ever-More Powder-Free Polymer-Coated Latex Examination Gloves Regulation Number: 880.6250 Regulation Name: Patient Examination Gloves Regulatory Class: I Product Code: LYY Dated: October 9, 2002 Received: October 21, 2002
Dear Mr. Cheng:
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 (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. 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.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting vour 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.
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Page 2 - Ms. Cheng
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); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. This letter will allow you to begin marketing your device as described in your Section 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), please contact the Office of Compliance at (301) 594-4618. 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" (21CFR Part 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html
Sincerely vours,
Susan Runnet
< Timothy A. Ulatowski Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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510 (K) Number (if known) : _ K 023523
and the same of the same of the same of the same
Euer-move Device Name : Powder-Free Polymer-Coated Latex Examination Gloves
......
Indication For use : .
A powder-Free patient examination glove is a disposable device made of natural rubber latex that may bear a trace amount of glove powder and is intended to be worn on the examiner's hand or finger's for medical purposes to provide a barrier against potentially infectious materials and other contaminants.
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE)
StB for Clun
(Division Sign-Off) Division of Anesthesiology, General Hospital, Infection Control, Dental Devices
510(k) Number ________________________________________________________________________________________________________________________________________________________________
OR Over The Counter Use Prescription Use (Per 21 CFR 801.109) (Optional Format1-2-95)
§ 880.6250 Non-powdered patient examination glove.
(a)
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.(b)
Classification. Class I (general controls). The device, when it is a finger cot, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 880.9.