ClearanceBrief
510(k) K882163 ยท JJN Apparatus, Electrophoresis, For Clinical Use

HELENA REP GEL PROCESSOR

ApplicantHelena Laboratories, Beaumont TX, US
DecisionSubstantially Equivalent, Jun 20, 1988
ReceivedMay 24, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882163

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.