ClearanceBrief
510(k) K822213 ยท BTM Ventilator, Emergency, Manual (Resuscitator)

SIEMENS-ELEMA AB AGA REVIVATOR

ApplicantSiemens Elema AB, Walker MI, US
DecisionSubstantially Equivalent, Oct 28, 1982
ReceivedJul 26, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K822213

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.