SEMPERMED SUPREME, SIZES 5.5, 6, 6.5, 7, 7.5, 8, 8.5, AND 9— 510(k) K013560
Substantially EquivalentSemperit 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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More clearances from Semperit Technische Produkte Gesellshaft
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