510(k) K902207 ยท DQX Wire, Guide, Catheter
ACS .010 HI-TORQUE INTER. AND STANDARD GUIDE WIRE
| Applicant | Advanced Cardiovascular Systems, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Aug 8, 1990 |
| Received | May 16, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902207
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.