ClearanceBrief
510(k) K093766 ยท DSI Detector And Alarm, Arrhythmia

VITALOGIK 6000/6500

ApplicantMennen Medical , Ltd., Yavne, Rehovot, IL
DecisionSubstantially Equivalent, May 7, 2010
ReceivedDec 7, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K093766

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.