ClearanceBrief
510(k) K220111 ยท BZQ Monitor, Breathing Frequency

RespiraSense

ApplicantPmd Solutions, Cork, IE
DecisionSubstantially Equivalent, Oct 7, 2022
ReceivedJan 13, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220111

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.