ClearanceBrief
510(k) K950853 ยท CBK Ventilator, Continuous, Facility Use

OPTIONAL DISPLAY AND SOFTWARE FOR DRAGER VENTILATORS

ApplicantDrager, Inc., Chantilly VA, US
DecisionSubstantially Equivalent - Subject to Tracking Reg., Nov 5, 1996
ReceivedFeb 27, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950853

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.