ANSELL CONFORM GREEN EXAMINATION GLOVES— 510(k) K897081

Name: FDA 510(k) clearance K897081
Creator: U.S. Food and Drug Administration
Published: 1990-03-26

Substantially Equivalent

Ansell, Inc.

FDA 510(k) clearance K897081 for ANSELL CONFORM GREEN EXAMINATION GLOVES, Substantially Equivalent on 1990-03-26. Applicant: Ansell, Inc.. Device class: 1.

Clearance details

Applicant: Ansell, Inc.
Product code: Code LYZ
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1989-12-19
Decision date: 1990-03-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Thailand, TH

Download summary PDF View on FDA.gov ↗

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