ClearanceBrief
510(k) K792105 ยท DSF Recorder, Paper Chart

CRITIKON DUAL CHANNEL RECORDER

ApplicantCritikon Company, LLC, Mchenry IL, US
DecisionSubstantially Equivalent, Oct 26, 1979
ReceivedOct 22, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K792105

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.