De Novo
DEN180028: 23andMe Personal Genome Service (PGS) Pharmacogenetic Reports
FDA De Novo · 23andme, inc. · decided Oct 31, 2018
Key facts
| De Novo number | DEN180028 |
|---|---|
| Device name | 23andMe Personal Genome Service (PGS) Pharmacogenetic Reports |
| Applicant | 23andme, inc. |
| Product code | QDJ |
| Date received | Jun 5, 2018 |
| Decision date | Oct 31, 2018 |
| Decision | granted (DENG) |
| FDA classification | Class II |
| Review panel | Clinical Chemistry |
| FEI number | 3007699459 |
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: