510(k) K023320 ยท DQY Catheter, Percutaneous
AGILTRAC .035 PERIPHERAL DILATATION CATHETER
| Applicant | Guidant Corp., Menlo Park CA, US |
| Decision | Substantially Equivalent, Dec 10, 2002 |
| Received | Oct 4, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023320
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.