PRE-POWDERED VINYL PATIENT EXAMINATION GLOVES— 510(k) K992271

Name: FDA 510(k) clearance K992271
Creator: U.S. Food and Drug Administration
Published: 1999-10-01

Substantially Equivalent

Shanghai Cosmos Corp.

FDA 510(k) clearance K992271 for PRE-POWDERED VINYL PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1999-10-01. Applicant: Shanghai Cosmos Corp.. Device class: 1.

Clearance details

Applicant: Shanghai Cosmos Corp.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1999-07-07
Decision date: 1999-10-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck,, NY, US

Download summary PDF View on FDA.gov ↗

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