510(k) K991152 ยท DQX Wire, Guide, Catheter
HI-TORQUE BALANCE TREK GUIDE WIRE
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Substantially Equivalent, Apr 29, 1999 |
| Received | Apr 6, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K991152
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.