510(k) K850075 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
SCIMED PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY DILAT
| Applicant | Scimed Life Systems, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Apr 10, 1985 |
| Received | Jan 9, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850075
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.