ClearanceBrief
510(k) K950169 ยท MQA Anti-Ribosomal P Antibodies

RIBOSOMAL P EIA TEST SYSTEM

ApplicantHogan & Hartson, Washington, D.C. DC, US
DecisionSubstantially Equivalent, May 23, 1996
ReceivedJan 17, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950169

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.