510(k) K862360 ยท DQX Wire, Guide, Catheter
ACS HI-TORQUE FLEX-T GUIDE WIRE
| Applicant | Advanced Cardiovascular Systems, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Sep 11, 1986 |
| Received | Jun 23, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862360
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.