510(k) K120372 ยท LRK Device, Anti-Snoring
DR GREENBURGS HYBRID VACUUM
| Applicant | Always More Marketing, Inc., Las Vegas NV, US |
| Decision | Substantially Equivalent, Jun 27, 2012 |
| Received | Feb 6, 2012 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K120372
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.