SEMPERMED SURGEON'S GLOVES— 510(k) K900587

Name: FDA 510(k) clearance K900587
Creator: U.S. Food and Drug Administration
Published: 1990-07-03

Substantially Equivalent

Semperit Industrial Products

FDA 510(k) clearance K900587 for SEMPERMED SURGEON'S GLOVES, Substantially Equivalent on 1990-07-03. Applicant: Semperit Industrial Products. Device class: 1.

Clearance details

Applicant: Semperit Industrial Products
Product code: Code KGO
Device class: Class 1
Regulation: 21 CFR 878.4460
Advisory panel: General, Plastic Surgery
Date received: 1990-02-07
Decision date: 1990-07-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montvale, NJ, US

Download summary PDF View on FDA.gov ↗

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