510(k) K972078 ยท EMX Balloon, Epistaxis
POST-STOP EPISTAXIS CATHETER
| Applicant | Boston Medical Products, Inc., Westborough MA, US |
| Decision | Substantially Equivalent, Jul 10, 1997 |
| Received | Jun 3, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972078
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.