ClearanceBrief
510(k) K880016 ยท DCK C-Reactive Protein, Antigen, Antiserum, And Control

MODIFIED CRP LATEX TEST

ApplicantSclavo, Inc., Wayne NJ, US
DecisionSubstantially Equivalent, Feb 25, 1988
ReceivedJan 5, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880016

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.