510(k) K152183 ยท FMI Needle, Hypodermic, Single Lumen
EXELINT SecureTouch Safety Hypodermic Needle
| Applicant | Exelint International, Co., Redondo Beach CA, US |
| Decision | Substantially Equivalent, Nov 2, 2015 |
| Received | Aug 5, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152183
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.