510(k) K103004 ยท LRK Device, Anti-Snoring
SNORE GUARD
| Applicant | Ranir, LLC, Washington DC, US |
| Decision | Substantially Equivalent, Feb 25, 2011 |
| Received | Oct 8, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K103004
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.