ClearanceBrief
510(k) K103427 ยท DPS Electrocardiograph

MOBILEECG SYSTEM

ApplicantMemtec Corp., Salem NH, US
DecisionSubstantially Equivalent, Mar 24, 2011
ReceivedNov 22, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K103427

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.