510(k) K023223 ยท DQY Catheter, Percutaneous
MODIFICATION TO LUMEND FRONTRUNNER CTO CATHETER
| Applicant | Lumend, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Oct 24, 2002 |
| Received | Sep 27, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K023223
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.