510(k) K033535 ยท PDU Catheter For Crossing Total Occlusions
LUMEND FRONTRUNNER CTO CATHETER AND ACCESSORIES
| Applicant | Lumend, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Jan 7, 2004 |
| Received | Nov 10, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K033535
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.