510(k) K810995 ยท FMF Syringe, Piston
PREFILLED PULSATOR SYRINGE
| Applicant | Concord Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 21, 1981 |
| Received | Apr 13, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810995
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.