510(k) K833248 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
LOW PROFILE STEERABLE-INTRAOPERATIVE
| Applicant | Advanced Cardiovascular Systems, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Dec 22, 1983 |
| Received | Sep 15, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833248
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.