SEMPERMED SUPREME, SIZES 5.5, 6, 6.5, 7, 7.5, 8, 8.5, AND 9— 510(k) K013560

Substantially Equivalent

Semperit Technische Produkte Gesellshaft

FDA 510(k) clearance K013560 for SEMPERMED SUPREME, SIZES 5.5, 6, 6.5, 7, 7.5, 8, 8.5, AND 9, Substantially Equivalent on 2002-01-16. 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
Decision date
Decision
Substantially Equivalent
Clearance type
Abbreviated
Location
Apharetta, GA, US
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