Cleared Traditional

K161074 - Powder Free Nitrile Examination Gloves Flock-Lined, Black Color (FDA 510(k) Clearance)

Nov 2016
Decision
213d
Days
Class 1
Risk

K161074 is an FDA 510(k) clearance for the Powder Free Nitrile Examination Gloves Flock-Lined, Black Color. This device is classified as a Polymer Patient Examination Glove (Class I - General Controls, product code LZA).

Submitted by Shen Wei (Usa), Inc. (Union City, US). The FDA issued a Cleared decision on November 17, 2016, 213 days after receiving the submission on April 18, 2016.

This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 880.6250. A Nitrile (or Polymer) Patient Examination Glove Is A Disposable Device Made Of Nitrile Rubber Or Synthetic Polymers That May Or May Not Bear A Trace Amount Of Residual Powder, And Is Intended To Be Worn On The Hand For Medical Purposes To Provide A Barrier Against Potentially Infectious Materials And Other Contaminants..

Submission Details

510(k) Number K161074 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 18, 2016
Decision Date November 17, 2016
Days to Decision 213 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF

Device Classification

Product Code LZA — Polymer Patient Examination Glove
Device Class Class I - General Controls
CFR Regulation 21 CFR 880.6250
Definition A Nitrile (or Polymer) Patient Examination Glove Is A Disposable Device Made Of Nitrile Rubber Or Synthetic Polymers That May Or May Not Bear A Trace Amount Of Residual Powder, And Is Intended To Be Worn On The Hand For Medical Purposes To Provide A Barrier Against Potentially Infectious Materials And Other Contaminants.

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