510(k) K894374 ยท FMI Needle, Hypodermic, Single Lumen
BLOOD DRAWING NEEDLE
| Applicant | Pharma-Plast USA, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Sep 28, 1989 |
| Received | Jul 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894374
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.