FDA 510(k) Application Details - K801191

Device Classification Name Circuit, Breathing (W Connector, Adaptor, Y Piece)

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510(K) Number K801191
Device Name Circuit, Breathing (W Connector, Adaptor, Y Piece)
Applicant AIRLIFE, INC.

, US
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Regulation Number 868.5240

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Classification Product Code CAI
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Date Received 05/19/1980
Decision Date 05/28/1980
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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