510(k) K013284 ยท DQY Catheter, Percutaneous
LUMEND FRONTRUNNER CTO CORONARY CATHETER
| Applicant | Lumend, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Feb 11, 2002 |
| Received | Oct 2, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013284
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.