510(k) K960127 ยท GRM Antisera, All Groups, Salmonella Spp.
SAS SALMONELLA O FACTOR 22 ANTISERUM &/OR SAS SALMONELLA O GROUP G1 FACTOR 22 ANTISERUM
| Applicant | Sa Scientific, Inc., San Antonio TX, US |
| Decision | Substantially Equivalent, Mar 6, 1996 |
| Received | Jan 11, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960127
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.