ClearanceBrief
510(k) K900260 ยท BTM Ventilator, Emergency, Manual (Resuscitator)

AMBU LIFE KEY AND AMBU RES-CUE KEY

ApplicantAmbu, Inc., Hanover MD, US
DecisionSubstantially Equivalent, Jun 8, 1990
ReceivedJan 17, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900260

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.