510(k) K942333 ยท DQX Wire, Guide, Catheter
SCIMED EN TRE' III PTCA GUIDE WIRE
| Applicant | Scimed Life Systems, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Aug 31, 1994 |
| Received | May 16, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942333
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.