SINOVENT MAXILLARY SINUS DRAINAGE SYSTEM— 510(k) K896630
Substantially EquivalentAtos Medical AB
FDA 510(k) clearance K896630 for SINOVENT MAXILLARY SINUS DRAINAGE SYSTEM, Substantially Equivalent on 1990-06-06. Applicant: Atos Medical AB. Device class: 1.
Clearance details
- Applicant
- Atos Medical AB
- Product code
- Code KAM
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Potomac, MD, US
Recent devices under product code KAM
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