ClearanceBrief
510(k) K782174 ยท CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)

PRESSURE ALARM

ApplicantThompson Respiration Products, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 22, 1979
ReceivedDec 19, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K782174

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.