FDA 510(k), K912723, POSEY CUFFLATOR

FDA 510(k), K912723, POSEY CUFFLATOR

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510(K) Number: K912723
Device Name: POSEY CUFFLATOR
Manufacturer: POSEY CO.
Device Classification Name: cuff, tracheal tube, inflatable
Regulation Number: 868.5750
Classification Product Code: BSK
Date Received: 06/19/1991
Decision Date: 07/20/1991
Regulation Medical Specialty: Anesthesiology

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