ClearanceBrief
510(k) K802054 ยท CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)

TRAVENOL ULTRASONIC NEBULIZER CUPS

ApplicantTravenol Laboratories, S.A., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 1, 1980
ReceivedAug 25, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802054

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.