510(k) K960933 ยท FMI Needle, Hypodermic, Single Lumen
BIO-PLEXUS NEEDLE DISPOSAL CONTAINER
| Applicant | Bio-Plexus, Inc., Tolland CT, US |
| Decision | Substantially Equivalent, Aug 28, 1996 |
| Received | Mar 7, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960933
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.