510(k) K941020 ยท FMF Syringe, Piston
DRUG RECONSTITUTION FILTER DEVICE
| Applicant | Gelman Sciences, Inc., Ann Arbor MI, US |
| Decision | Substantially Equivalent, Aug 10, 1994 |
| Received | Mar 3, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941020
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.