510(k) K103076 ยท LRK Device, Anti-Snoring
DYNAFLEX
| Applicant | Dyna Flex, Austin TX, US |
| Decision | Substantially Equivalent, Feb 23, 2011 |
| Received | Oct 18, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103076
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.