(106 days)
A powder free nitrile 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.
Colored Powder Free And Polymer Coated Nitrile Examination Glove (White, Blue and Black)
This document is a 510(k) summary for a Nitrile Examination Glove. It is a regulatory clearance letter from the FDA, and as such, it does not contain the kind of detailed study information you are asking for (acceptance criteria for algorithmic performance, sample sizes for training/test sets, expert qualifications, ground truth establishment, MRMC studies, or standalone performance).
The purpose of a 510(k) submission for this type of Class I medical device (patient examination glove) is to demonstrate substantial equivalence to a legally marketed predicate device, not necessarily to prove specific performance metrics through detailed studies. The acceptance criteria for such a device would typically relate to physical properties (e.g., tensile strength, elongation, barrier integrity like pinhole rate) and biocompatibility, as well as labeling requirements. These are usually established through recognized consensus standards rather than clinical performance studies of an algorithm.
Therefore, I cannot extract the requested information from this document. The document primarily focuses on regulatory classification and clearance.
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Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002
AUG 3 2012
Mr. Patrick Leong Tekmedic (M) Sdn Bhd Plot 4. Tanjung Kling Industrial Area Taniung Bruas Jetty Taniung Kling Malacca, Malaysia 76400
Re: K121192
Trade/Device Name: Colored Powder Free and Polymer Coated Nitrile Examination Glove (White, Blue and Black) Regulation Number: 21 CFR 880.6250 Regulation Name: Patient Examination Glove Regulatory Class: I Product Code: LZA Dated: June 29, 2012 Received: July 2, 2012
Dear Mr. Leong:
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. 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.
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Page 2 - Mr. Leong
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 803); 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.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to
http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled. "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm.
Sincerely yours.
for. R. Bette
Anthony D. Watson, B.S., M.S., M.B.A. 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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Premarket Notification For Colored Powder Free And Polymer Coated Nitrile Examination Glove (White, Blue and Black)
4.0 Indication For Use Statement
K121192 510 (K) Number (if known) :___________________________________________________________________________________________________________________________________________________
Colored Powder Free And Polymer Coated Nitrile Device Name : Examination Glove (White, Blue and Black)
: A powder free nitrile examination glove is a disposable Indication For Use device intended for medical purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner.
Prescription Use Part 21 CFR 801 Subpart D
X Over-The-Counter Use (21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE OF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
$\frac{\text{Elizabeth}}{\text{(Division Sign-Off)}}$ F. Ramirez W.M.
Division of Anesthesiology, General Hospital Intection Control, Dental Devices
510(k) Number:
§ 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.