510(k) K140438 ยท PDU Catheter For Crossing Total Occlusions
MICRO GUIDE CATHETER ELITE
| Applicant | Cordis Corp., A Johnson & Johnson Co., Fremont CA, US |
| Decision | Substantially Equivalent, Nov 14, 2014 |
| Received | Feb 21, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140438
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.