De Novo
DEN180026: Bose Hearing Aid
FDA De Novo · bose corporation · decided Oct 5, 2018
Key facts
| De Novo number | DEN180026 |
|---|---|
| Device name | Bose Hearing Aid |
| Applicant | bose corporation |
| Product code | QDD |
| Date received | May 11, 2018 |
| Decision date | Oct 5, 2018 |
| Decision | granted (DENG) |
| FDA classification | Class II |
| Review panel | Ear, Nose, & Throat |
| FEI number | 3015489745 |
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: