ClearanceBrief
510(k) K812041 ยท CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)

VENTI-MONITOR MODEL 101

ApplicantMedix Medical Electronics (U.S.A.), Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 25, 1981
ReceivedJul 21, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812041

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.