ClearanceBrief
510(k) K983221 ยท DEW Igg, Antigen, Antiserum, Control

IGG

ApplicantAbbott Laboratories, Irving TX, US
DecisionSubstantially Equivalent, Nov 4, 1998
ReceivedSep 14, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983221

DateFirm and productCodeLinked 510(k)
May 16, 2018Abbott Laboratories, Inc
Immunoglobulin G is an in vitro diagnostic assay for the quantitative determination of immunoglobulin G in human serum or plasma. Antigen in the sample bonds to the specific antibody in the reagent, f
Terminated
DEWNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.