510(k) K102439 ยท DQY Catheter, Percutaneous
FUNNEL GUIDE CATHETER MODEL G1020608
| Applicant | Lazarus Effect, Inc., Felton CA, US |
| Decision | Substantially Equivalent, Jan 12, 2012 |
| Received | Aug 26, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102439
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.