510(k) K931171 ยท DQX Wire, Guide, Catheter
DOC-TITE(TM) GUIDE WIRE EXTENSION
| Applicant | Advanced Cardiovascular Systems, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Jun 4, 1993 |
| Received | Mar 8, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931171
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.