CABOCHON SYSTEM— 510(k) DEN110004
UnknownCabochon Aesthetics, Inc.
FDA 510(k) clearance DEN110004 for CABOCHON SYSTEM, Unknown on 2013-07-12. Applicant: Cabochon Aesthetics, Inc.. Device class: 2.
Clearance details
- Applicant
- Cabochon Aesthetics, Inc.
- Product code
- Code OUP
- Device class
- Class 2
- Regulation
- 21 CFR 878.4790
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- Menlo Park, CA, US
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