510(k) K170053 ยท LRK Device, Anti-Snoring
Meridian PM
| Applicant | The Center For Craniofacial & Dental Sleep Medicine, Sugarland TX, US |
| Decision | Substantially Equivalent, Nov 28, 2017 |
| Received | Jan 5, 2017 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K170053
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.