510(k) K073401 ยท MJV Device, Inflation, Middle Ear
EARPOPPER, MODEL EP-2000, EP-2100, EP-3000
| Applicant | Micromedics, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Mar 14, 2008 |
| Received | Dec 4, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073401
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.