ClearanceBrief
510(k) K822115 ยท CKG Radioimmunoassay, Acth

SERAGAN ACTH125 I-RIA KIT

ApplicantSeragen Diagnostics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 18, 1982
ReceivedJul 19, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K822115

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.