510(k) K954251 ยท DQY Catheter, Percutaneous
5F ENVOY GUIDING CATHETER (MODIFICATION)
| Applicant | Cordis Neurovascular, Inc., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Oct 23, 1995 |
| Received | Aug 24, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954251
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.