510(k) K012002 ยท DQY Catheter, Percutaneous
VIKING OPTIMA GUIDING CATHETER
| Applicant | Guidant Corp., Temecula CA, US |
| Decision | Substantially Equivalent, Jul 26, 2001 |
| Received | Jun 27, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012002
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.