510(k) K961980 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
BIPORE BALLOON DILATATION CATHETER
| Applicant | Bipore, Inc., Northvale NJ, US |
| Decision | Substantially Equivalent, Sep 12, 1996 |
| Received | May 20, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961980
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.