ClearanceBrief
510(k) K222389 ยท DQK Computer, Diagnostic, Programmable

ZEUS System

ApplicantiRhythm Technologies, Inc., San Francisco CA, US
DecisionSubstantially Equivalent, Feb 15, 2023
ReceivedAug 8, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K222389

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.