510(k) K052514 ยท PDU Catheter For Crossing Total Occlusions
CLIRPATH TURBO PLUS EXCIMER LASER CATHETERS, MODELS 314-151, 314-159, 317-152, 317-156, 320-006, 320-159, 323-001
| Applicant | Spectranetics Corp., Colorado Springs CO, US |
| Decision | Substantially Equivalent, Oct 19, 2005 |
| Received | Sep 14, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052514
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.