ClearanceBrief
510(k) K182093 ยท DPS Electrocardiograph

ZOLL ECG Analysis Software

ApplicantZoll Manufacturing Corporation, Pittsburgh PA, US
DecisionSubstantially Equivalent, Jan 28, 2019
ReceivedAug 3, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K182093

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.