ClearanceBrief
510(k) K863822 ยท DGC Ige, Antigen, Antiserum, Control

ENZYMUN-TEST(R) IGE

ApplicantBoehringer Mannheim Corp., Indianapolis IN, US
DecisionSubstantially Equivalent, Oct 29, 1986
ReceivedSep 30, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863822

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.