510(k) K082339 ยท DQY Catheter, Percutaneous
ENABLER-P SUPPORT CATHETER
| Applicant | Endocross, Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Nov 20, 2008 |
| Received | Aug 14, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082339
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.