ClearanceBrief
510(k) K223818 ยท JEH Plethysmograph, Volume

Model 9160 VitaloQUB

ApplicantVitalograph Ireland, Ltd., Ennis Co Clare, IE
DecisionSubstantially Equivalent, May 25, 2023
ReceivedDec 21, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K223818

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.