510(k) K102979 ยท DQY Catheter, Percutaneous
NEXGEN PERIPHERAL GUIDE CATHETER
| Applicant | Nexgen Medical Systems, Inc., Melbourne FL, US |
| Decision | Substantially Equivalent, Jan 18, 2011 |
| Received | Oct 6, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102979
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.