FDA 510(k) Application Details - K842340

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

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510(K) Number K842340
Device Name Humidifier, Respiratory Gas, (Direct Patient Interface)
Applicant BEAR MEDICAL SYSTEMS, INC.

, US
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Regulation Number 868.5450

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Classification Product Code BTT
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Date Received 06/14/1984
Decision Date 07/17/1984
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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