FDA 510(k) Application Details - K820878

Device Classification Name Humidifier, Respiratory Gas, (Direct Patient Interface)

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510(K) Number K820878
Device Name Humidifier, Respiratory Gas, (Direct Patient Interface)
Applicant RCI, INC.

, US
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Regulation Number 868.5450

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Classification Product Code BTT
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Date Received 03/30/1982
Decision Date 05/03/1982
Decision SE - Substantially Equivalent
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee AN - Anesthesiology
Statement / Summary / Purged Status
Type Traditional
Reviewed By Third Party N
Expedited Review



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