510(k) K820449 ยท FMF Syringe, Piston
PHARMACEUTICALS MOD. 1CC-1,2,3 THRU 50CC
| Applicant | Abek Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 12, 1982 |
| Received | Feb 18, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820449
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.