510(k) K781220 · DEH Lambda, Antigen, Antiserum, Control

ANTI-HUMAN LAMBDA SERUM

Applicant	Icl Scientific, Mchenry IL, US
Decision	Substantially Equivalent, Jul 27, 1978
Received	Jul 17, 1978
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K781220

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.