ClearanceBrief
510(k) K142693 ยท DPS Electrocardiograph

ZywieAI Software Library

ApplicantZywie, Inc., Johns Creek GA, US
DecisionSubstantially Equivalent, Feb 20, 2015
ReceivedSep 22, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K142693

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.