AIRBRUSH LIPOSCULPTOR SYSTEM— 510(k) K031881
Substantially EquivalentBiosculpture Technology, Inc.
FDA 510(k) clearance K031881 for AIRBRUSH LIPOSCULPTOR SYSTEM, Substantially Equivalent on 2003-07-28. Applicant: Biosculpture Technology, Inc.. Device class: 2.
Clearance details
- Applicant
- Biosculpture Technology, Inc.
- Product code
- Code QPB
- Device class
- Class 2
- Regulation
- 21 CFR 878.5040
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
Recent devices under product code QPB
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