AIRSONETT AIR-4— 510(k) K130702
Substantially EquivalentAirsonett AB
FDA 510(k) clearance K130702 for AIRSONETT AIR-4, Substantially Equivalent on 2013-07-23. Applicant: Airsonett AB. Device class: 2.
Clearance details
- Applicant
- Airsonett AB
- Product code
- Code FRF
- Device class
- Class 2
- Regulation
- 21 CFR 880.5045
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Fridley, MN, US
Recent devices under product code FRF
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