510(k) K073318 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
BIPORE BALLOON DILATION CATHETER
| Applicant | Bipore, Inc., Northvale NJ, US |
| Decision | Substantially Equivalent, Jan 16, 2008 |
| Received | Nov 26, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K073318
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.