510(k) K960882 ยท FMF Syringe, Piston
CONTROL SYRINGE
| Applicant | Louisville Laboratories, Inc., Louisville KY, US |
| Decision | Substantially Equivalent, Jul 8, 1996 |
| Received | Feb 20, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960882
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.