ClearanceBrief
510(k) K990429 ยท CBK Ventilator, Continuous, Facility Use

MODIFICATION OF VENTURI VENTILATOR

ApplicantCardiopulmonary Corp., Milford CT, US
DecisionSubstantially Equivalent - Subject to Tracking Reg., Feb 24, 1999
ReceivedFeb 11, 1999
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K990429

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.