510(k) K844972 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
ADV CARDIO SYS DBL LUMEN BALLOON DILATA CATHETER
| Applicant | Advanced Cardiovascular Systems, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, May 16, 1985 |
| Received | Dec 24, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844972
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.