510(k) K023300 ยท DQX Wire, Guide, Catheter
HI-TORQUE WHISPER LS; HI-TORQUE WHISPER MS; HI-TORQUE WHISPER MS CS-J; HI-TORQUE WHISPER ES; HI-TORQUE WHISPER ES CS-J
| Applicant | Guidant Corp., St Paul MN, US |
| Decision | Substantially Equivalent, Oct 28, 2002 |
| Received | Oct 3, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K023300
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.