510(k) K150187 ยท PDU Catheter For Crossing Total Occlusions
ELITECROSS Support Catheter
| Applicant | Cordis Corporation, A Johnson & Johnson Company, Fremont CA, US |
| Decision | Substantially Equivalent, May 19, 2015 |
| Received | Jan 27, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150187
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.