510(k) K852123 ยท DQX Wire, Guide, Catheter
WHOLEY HI-TORQUE GUIDE WIRES
| Applicant | Advanced Cardiovascular Systems, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Jun 19, 1985 |
| Received | May 15, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852123
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.