510(k) K020340 ยท DQX Wire, Guide, Catheter
MODIFICATION TO HI-TORQUE WHISPER LS AND MS GUIDE WIRES WITH HYDROCOAT HYDROPHILIC COATING
| Applicant | Guidant Corp., Temecula CA, US |
| Decision | Substantially Equivalent, Mar 1, 2002 |
| Received | Feb 1, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020340
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.