ClearanceBrief
510(k) K103640 ยท DPS Electrocardiograph

MIDMARK IQECG

ApplicantBrentwood Medical Technology Corp., Irvine CA, US
DecisionSubstantially Equivalent, Mar 22, 2011
ReceivedDec 13, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K103640

DateFirm and productCodeLinked 510(k)
Aug 25, 2026Midmark Corporation
Midmark IQecg Digital ECG, Model/Catalog Number: 4-000-0061, 4-000-0062 Software Version: Midmark IQecg Plugin versions starting with v10 and prior to v10.1.0.18.
Open, Classified
DPSNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.