ClearanceBrief
510(k) K873352 ยท JJN Apparatus, Electrophoresis, For Clinical Use

RAPID ELECTROPHORESIS SYSTEM (REP)

ApplicantHelena Laboratories, Beaumont TX, US
DecisionSubstantially Equivalent, Sep 8, 1987
ReceivedAug 20, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K873352

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.