Cabochon Aesthetics, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K134010 | CABOCHON SYSTEM | April 14, 2014 |
| DEN110004 | CABOCHON SYSTEM | July 12, 2013 |