ANSELL E.P. EXTRA-PROTECTION EXAMINATION GLOVES— 510(k) K895781

Name: FDA 510(k) clearance K895781
Creator: U.S. Food and Drug Administration
Published: 1990-03-09

Substantially Equivalent

Ansell Intl.

FDA 510(k) clearance K895781 for ANSELL E.P. EXTRA-PROTECTION EXAMINATION GLOVES, Substantially Equivalent on 1990-03-09. Applicant: Ansell Intl.. Device class: 1.

Clearance details

Applicant: Ansell Intl.
Product code: Code LZC
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1989-09-27
Decision date: 1990-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Melaka, MT

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.