510(k) K013638 ยท DQY Catheter, Percutaneous
MODIFICATION TO VIKING OPTIMA GUIDING CATHETER
| Applicant | Guidant Corp., Temecula CA, US |
| Decision | Substantially Equivalent, Dec 4, 2001 |
| Received | Nov 5, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K013638
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.