510(k) K843501 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
BALLOON DILATION CATHETER
| Applicant | Advanced Cardiovascular Systems, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Oct 4, 1984 |
| Received | Sep 6, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843501
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.