510(k) K973563 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
BIPORE BALLOON DILATATION CATHETER
| Applicant | Bipore, Inc., Northvale NJ, US |
| Decision | Substantially Equivalent, Apr 1, 1998 |
| Received | Sep 19, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973563
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.