510(k) K013833 ยท DQX Wire, Guide, Catheter
HI-TOQUE BALANCE MIDDLEWEIGHT UNIVERSAL GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING, #1009659,1009659J, 1009660, 10096
| Applicant | Guidant Corp., Temecula CA, US |
| Decision | Substantially Equivalent, Jan 16, 2002 |
| Received | Nov 19, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013833
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.