510(k) K961251 ยท FMI Needle, Hypodermic, Single Lumen
PUNCTUR-GUARD WINGED SET
| Applicant | Bio-Plexus, Inc., Tolland CT, US |
| Decision | Substantially Equivalent, Jun 27, 1996 |
| Received | Apr 1, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961251
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.