De Novo
DEN090012: VIRULITE COLD SORE MACHINE
FDA De Novo · virulite llc · decided Oct 18, 2012
Key facts
| De Novo number | DEN090012 |
|---|---|
| Device name | VIRULITE COLD SORE MACHINE |
| Applicant | virulite llc |
| Product code | OKJ |
| Date received | Jun 30, 2009 |
| Decision date | Oct 18, 2012 |
| Decision | granted (DENG) |
| FDA classification | Class II |
| Review panel | General & Plastic Surgery |
| FEI number | 3008660757 |
At a glance
- 1–9 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: