510(k) K040067 ยท PDU Catheter For Crossing Total Occlusions
CLIRPATH EXCIMER LASER CATHETER
| Applicant | Spectranetics Corp., Colorado Springs CO, US |
| Decision | Substantially Equivalent, Apr 27, 2004 |
| Received | Jan 14, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K040067
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.