510(k) K983346 ยท DQX Wire, Guide, Catheter
STANDARD 0.025 STRAIGHT, STANDARD 0.025 ANGLED, STANDARD 0.032 STRAIGHT, STANDARD 0.032 ANGLED, SOFT 0.035 STRAIGHT, SOF
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Substantially Equivalent, Mar 23, 1999 |
| Received | Sep 23, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983346
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.