ClearanceBrief
510(k) K942938 ยท CBK Ventilator, Continuous, Facility Use

CROSSVENT-4 VENTILATOR

ApplicantBio-Med Devices, Inc., Guilford CT, US
DecisionSubstantially Equivalent - Subject to Tracking Reg., Sep 19, 1995
ReceivedJun 22, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K942938

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.