510(k) K875064 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
SCIMED INFLATION DEVICE, MODEL SM 2000
| Applicant | Scimed Life Systems, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 29, 1988 |
| Received | Dec 9, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875064
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.