510(k) K020161 ยท DQY Catheter, Percutaneous
AGILTRAC .018 PERIPHERAL DILATATION CATHETER
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Substantially Equivalent, Feb 22, 2002 |
| Received | Jan 17, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020161
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.