510(k) K021283 ยท DQO Catheter, Intravascular, Diagnostic
GUIDANT BALLOON CATHETER, SEVERAL MODELS
| Applicant | Guidant Corp., St Paul MN, US |
| Decision | Substantially Equivalent, May 2, 2002 |
| Received | Apr 18, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021283
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.