510(k) K120665 ยท LWF Dilator, Nasal
INVENT SNORING DEVICE
| Applicant | Ventus Medical, Inc., Hillsborough CA, US |
| Decision | Substantially Equivalent, Jun 12, 2012 |
| Received | Mar 5, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120665
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.