510(k) K992169 ยท DQX Wire, Guide, Catheter
ACS HI-TORQUE CROSS-IT 400XT GUIDE WIRE
| Applicant | Advanced Cardiovascular Systems, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Oct 28, 1999 |
| Received | Jun 28, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992169
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.