510(k) K031005 ยท PDU Catheter For Crossing Total Occlusions
LUMEND FRONTRUNNER GW CTO CATHETER
| Applicant | Lumend, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Jun 18, 2003 |
| Received | Mar 31, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031005
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.