510(k) K951965 ยท DEH Lambda, Antigen, Antiserum, Control
DAKO LABELED STREPTAVIDIN-BIOTIN 2 KIT, AND ENVISION
| Applicant | Dako Corp., Carpinteria CA, US |
| Decision | Substantially Equivalent, Jul 5, 1996 |
| Received | Apr 27, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951965
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.