510(k) K082143 ยท PDU Catheter For Crossing Total Occlusions
MICRO GUIDE CATHETER XP
| Applicant | Cordis Corp., Warren NJ, US |
| Decision | Substantially Equivalent, Aug 25, 2008 |
| Received | Jul 30, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082143
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.