ClearanceBrief
510(k) K062282 ยท DPS Electrocardiograph

MONEBO AUTOMATED ECG ANALYSIS AND INTERPRETATION SOFTWARE LIBRARY, VERSION 3.0

ApplicantMonebo Technologies, Inc., Austin TX, US
DecisionSubstantially Equivalent, Mar 22, 2007
ReceivedAug 7, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K062282

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.