SEMPERMED SURGEONS' GLOVES - SUPREME— 510(k) K981096

Name: FDA 510(k) clearance K981096
Creator: U.S. Food and Drug Administration
Published: 1998-10-29

Substantially Equivalent

Semperit Technische Produkte Gesellshaft

FDA 510(k) clearance K981096 for SEMPERMED SURGEONS' GLOVES - SUPREME, Substantially Equivalent on 1998-10-29. Applicant: Semperit Technische Produkte Gesellshaft. Device class: 1.

Clearance details

Applicant: Semperit Technische Produkte Gesellshaft
Product code: Code KGO
Device class: Class 1
Regulation: 21 CFR 878.4460
Advisory panel: General, Plastic Surgery
Date received: 1998-03-25
Decision date: 1998-10-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vienna, AT

Download summary PDF View on FDA.gov ↗

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