510(k) K061453 ยท DQX Wire, Guide, Catheter
HI-TORQUE WHISPER VIEW GUIDE WIRE
| Applicant | Guidant Corp., St Paul MN, US |
| Decision | Substantially Equivalent, Jun 22, 2006 |
| Received | May 25, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K061453
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.