510(k) K041293 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
BIOPORE BALLOON DILATION CATHETER
| Applicant | Bipore, Inc., Northvale NJ, US |
| Decision | Substantially Equivalent, Jul 9, 2004 |
| Received | May 14, 2004 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K041293
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.