De Novo
DEN190037: NaviCam Capsule Endoscope System with NaviCam Stomach Capsule
FDA De Novo · anx robotica, inc. · decided May 22, 2020
Key facts
| De Novo number | DEN190037 |
|---|---|
| Device name | NaviCam Capsule Endoscope System with NaviCam Stomach Capsule |
| Applicant | anx robotica, inc. |
| Product code | QKZ |
| Date received | Aug 13, 2019 |
| Decision date | May 22, 2020 |
| Decision | granted (DENG) |
| FDA classification | Class II |
| Review panel | Gastroenterology & Urology |
| FEI number | 3016544248 |
At a glance
- 1–9 Later 510(k)s citing this De Novo
- 1–9 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: