510(k) K831403 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
LOW PROFILE STEERABLE BALLOON DILATA
| Applicant | Advanced Cardiovascular Systems, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jun 8, 1983 |
| Received | May 2, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831403
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.