510(k) K122249 ยท FMI Needle, Hypodermic, Single Lumen
TERUMO SURGUARD3 SAFETY NEEDLE & HYPODERMIC SYRINGE WITH SAFETY NEEDLE
| Applicant | Terumo (Philippines) Corporation, Elkton MD, US |
| Decision | Substantially Equivalent, Aug 28, 2012 |
| Received | Jul 27, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K122249
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.