ClearanceBrief
510(k) K802231 ยท BTM Ventilator, Emergency, Manual (Resuscitator)

AIR VIVA II

ApplicantGeneral Medical Co., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 10, 1980
ReceivedSep 15, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802231

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.