ClearanceBrief
510(k) K803281 ยท JJN Apparatus, Electrophoresis, For Clinical Use

AUTOMATED ELECTROPHORESIS SYSTEM

ApplicantHelena Laboratories, Mchenry IL, US
DecisionSubstantially Equivalent, Jan 16, 1981
ReceivedDec 29, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K803281

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.