510(k) K092174 ยท DQY Catheter, Percutaneous
ENABLER-P CATHETER SYSTEM, MODEL 3000
| Applicant | Endocross, Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Dec 30, 2009 |
| Received | Jul 21, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092174
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.