510(k) K791283 ยท DEH Lambda, Antigen, Antiserum, Control
ANTI-HUMAN LAMBDA SERUM
| Applicant | Diagnostica, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 27, 1979 |
| Received | Jul 10, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791283
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.