De Novo
DEN150048: gammaCore Non-invasive Vagus Nerve Stimulator
FDA De Novo · electrocore, llc · decided Apr 14, 2017
Key facts
| De Novo number | DEN150048 |
|---|---|
| Device name | gammaCore Non-invasive Vagus Nerve Stimulator |
| Applicant | electrocore, llc |
| Product code | PKR |
| Date received | Oct 16, 2015 |
| Decision date | Apr 14, 2017 |
| Decision | granted (DENG) |
| FDA classification | Class II |
| Review panel | Neurology |
| FEI number | 3015529603 |
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: