510(k) K924646 ยท KNQ Dilator, Esophageal
OVER THE GUIDEWIRE DILATATION SYSTEM
| Applicant | Medovations, Inc., Germantown WI, US |
| Decision | Substantially Equivalent, Dec 5, 1994 |
| Received | Sep 14, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924646
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.