510(k) K030019 ยท DQX Wire, Guide, Catheter
MODIFICATION TO HI-TORQUE WHISPER GUIDEWIRE
| Applicant | Guidant Corp., St Paul MN, US |
| Decision | Substantially Equivalent, Jan 24, 2003 |
| Received | Jan 3, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030019
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.