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..
Clearance details
- Applicant
- Biosculpture Technology, Inc.
- Product code
- Code QPB
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.