510(k) K111948 ยท FIE Needle, Fistula
WINGEATER V2
| Applicant | JMS North America Corporation, Crofton MD, US |
| Decision | Substantially Equivalent, Oct 24, 2011 |
| Received | Jul 8, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K111948
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.