510(k) K013581 ยท DQY Catheter, Percutaneous
CORDIS AVIATOR PERIPHERAL DILATATION CATHETER
| Applicant | Cordis, A Johnson & Johnson Co., Warren NJ, US |
| Decision | Substantially Equivalent, Nov 28, 2001 |
| Received | Oct 29, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K013581
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.