510(k) K935161 ยท DEH Lambda, Antigen, Antiserum, Control
KERATIN PRIMARY ANTIBODY
| Applicant | Ventana Medical Systems, Inc., Tucson AZ, US |
| Decision | Substantially Equivalent, Mar 22, 1996 |
| Received | Oct 29, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935161
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.