POWDERED VINYL PATIENT EXAMINATION GLOVES, WHITE— 510(k) K070040

Name: FDA 510(k) clearance K070040
Creator: U.S. Food and Drug Administration
Published: 2007-01-26

Substantially Equivalent

Super Safe Plastic Products Co., Ltd.

FDA 510(k) clearance K070040 for POWDERED VINYL PATIENT EXAMINATION GLOVES, WHITE, Substantially Equivalent on 2007-01-26. Applicant: Super Safe Plastic Products Co., Ltd.. Device class: 1.

Clearance details

Applicant: Super Safe Plastic Products Co., Ltd.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2007-01-03
Decision date: 2007-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chino, CA, US

Download summary PDF View on FDA.gov ↗

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K070043 — POWDER FREE VINYL PATIENT EXAMINATION GLOVES, WHITE2007-02-08
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