ClearanceBrief
510(k) K830230 ยท CBK Ventilator, Continuous, Facility Use

PROGRAMMABLE VENTILATOR

ApplicantBio-Med Devices, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 9, 1983
ReceivedJan 28, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830230

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.