ClearanceBrief
510(k) K080141 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

PC ECG 1200W SYSTEM

ApplicantNorav Medical , Ltd., Mitzpe Aviv, IL
DecisionSubstantially Equivalent, Apr 25, 2008
ReceivedJan 22, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K080141

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.