De Novo
DEN130051: PEDIATRIC VISION SCANNER
FDA De Novo · rebiscan, inc. · decided Jun 8, 2016
Key facts
| De Novo number | DEN130051 |
|---|---|
| Device name | PEDIATRIC VISION SCANNER |
| Applicant | rebiscan, inc. |
| Product code | PMW |
| Date received | Dec 13, 2013 |
| Decision date | Jun 8, 2016 |
| Decision | granted (DENG) |
| FDA classification | Class II |
| Review panel | Ophthalmic |
| FEI number | 3014522421 |
At a glance
- None Later 510(k)s citing this De Novo
- None UDI device identifiers (GUDID)
- 1–9 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: