510(k) K963748 ยท FMI Needle, Hypodermic, Single Lumen
BIO-PLEXUS DROP-IT NEEDLE HOLDER
| Applicant | Bio-Plexus, Inc., Vernon CT, US |
| Decision | Substantially Equivalent, Jun 6, 1997 |
| Received | Sep 17, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963748
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.