510(k) K915168 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
PROFLEX 5
| Applicant | Peripheral Systems Group, Mountain View CA, US |
| Decision | Substantially Equivalent, Feb 19, 1992 |
| Received | Nov 15, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915168
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.