ClearanceBrief
510(k) K900313 ยท CBK Ventilator, Continuous, Facility Use

PERCUSSIONAIRE(R) VDR-3 IMV PERCUS/RESPIR 1250 MIN

ApplicantPercussionaire Corp., Sandpoint ID, US
DecisionSubstantially Equivalent, Oct 26, 1990
ReceivedJan 22, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900313

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.