510(k) K983650 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
BIPORE BALLOON DILATATION CATHETER
| Applicant | Bipore, Inc., Northvale NJ, US |
| Decision | Substantially Equivalent, Feb 17, 1999 |
| Received | Oct 16, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983650
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.