510(k) K052296 ยท PDU Catheter For Crossing Total Occlusions
CLIRPATH TURBO EXCIMER LASER CATHETERS
| Applicant | Spectranetics Corp., Colorado Springs CO, US |
| Decision | Substantially Equivalent, Sep 2, 2005 |
| Received | Aug 23, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052296
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.