510(k) K950216 ยท DQX Wire, Guide, Catheter
SCIMED CHOICE PT PLUS(RM) PTCA GUIDE WIRE
| Applicant | Scimed Life Systems, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Jun 22, 1995 |
| Received | Jan 19, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950216
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.