ClearanceBrief
510(k) K182292 ยท CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)

VORTRAN APM-Plus

ApplicantVortran Medical Technology 1, Inc., Sacramento CA, US
DecisionSubstantially Equivalent, Sep 18, 2019
ReceivedAug 23, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K182292

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.