510(k) K840490 ยท FMF Syringe, Piston
FLUID REMOVAL ASSEMBLY
| Applicant | Ackrad Laboratories, Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 17, 1984 |
| Received | Feb 6, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840490
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.