510(k) K852442 ยท FMI Needle, Hypodermic, Single Lumen
PHARMA-PLAST NEEDLE
| Applicant | Pharma-Plast USA, Inc., Canada H3a 2n4, CA |
| Decision | Substantially Equivalent, Sep 20, 1985 |
| Received | Jun 10, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852442
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.