510(k) K152362 ยท FMI Needle, Hypodermic, Single Lumen
Terumo SurGuard 3 Safety Hypodermic Needle
| Applicant | Terumo (Philippines) Corporation, Binan, PH |
| Decision | Substantially Equivalent, Oct 16, 2015 |
| Received | Aug 20, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K152362
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.