510(k) K973038 ยท LRK Device, Anti-Snoring
ADJUSTABLE THERASNORE
| Applicant | Distar, Inc., Winchester VA, US |
| Decision | Substantially Equivalent, Nov 12, 1997 |
| Received | Aug 14, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973038
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.