ClearanceBrief
510(k) K183322 ยท DPS Electrocardiograph

physIQ Heart Rhythm and Respiratory Module

ApplicantPhysiq, Inc., Naperville IL, US
DecisionSubstantially Equivalent, Jul 10, 2019
ReceivedNov 30, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K183322

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.