510(k) K895179 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
ACCESSOR PERIPHERAL DILATING GUIDE WIRE
| Applicant | Peripheral Systems Group, Mountain View CA, US |
| Decision | Substantially Equivalent, Feb 28, 1990 |
| Received | Aug 10, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895179
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.