PLASMAIR, MODEL T2006— 510(k) K070722
Substantially EquivalentAirinspace B.V.
FDA 510(k) clearance K070722 for PLASMAIR, MODEL T2006, Substantially Equivalent on 2007-12-14. Applicant: Airinspace B.V.. Device class: 2.
Clearance details
- Applicant
- Airinspace B.V.
- 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
- Leesburg, VA, US
Recent devices under product code FRF
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