510(k) K972023 ยท LRK Device, Anti-Snoring
SLEEP-IN BONE SCREW SYSTEM
| Applicant | Influence, Inc., San Francisco CA, US |
| Decision | Substantially Equivalent, Aug 25, 1997 |
| Received | Jun 2, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972023
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.