De Novo
DEN110004: CABOCHON SYSTEM
FDA De Novo · cabochon aesthetics, inc. · decided Jul 12, 2013
Key facts
| De Novo number | DEN110004 |
|---|---|
| Device name | CABOCHON SYSTEM |
| Applicant | cabochon aesthetics, inc. |
| Product code | OUP |
| Date received | Oct 31, 2011 |
| Decision date | Jul 12, 2013 |
| Decision | granted (DENG) |
| FDA classification | Class II |
| Review panel | General & Plastic Surgery |
At a glance
- None Later 510(k)s citing this De Novo
- None UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
- No Decision summary on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About De Novo classification requests
The De Novo pathway classifies novel low- to moderate-risk devices that have no legally marketed predicate; each granted request creates a new classification regulation and product code.
Source: U.S. Food and Drug Administration (FDA), De Novo database · Source date: