ClearanceBrief
510(k) K884793 ยท CBK Ventilator, Continuous, Facility Use

ADVENT VENTILATOR

ApplicantOhmeda Medical, Columbia MD, US
DecisionSubstantially Equivalent, Jun 12, 1989
ReceivedNov 16, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884793

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.