ClearanceBrief
510(k) K900314 ยท CBK Ventilator, Continuous, Facility Use

PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN

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

Recalls that name K900314

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.