510(k) K112178 ยท FIE Needle, Fistula
JMS APHERESIS NEEDLE SET WINGEATER(R) V2
| Applicant | JMS North America Corporation, Crofton MD, US |
| Decision | Substantially Equivalent, Oct 27, 2011 |
| Received | Jul 28, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K112178
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.