510(k) K013687 ยท LRK Device, Anti-Snoring
NOSE BREATHE MOUTHPIECE FOR HEAVY SNORER
| Applicant | Steven K. Sue, Honolulu HI, US |
| Decision | Substantially Equivalent, May 28, 2002 |
| Received | Nov 7, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013687
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.