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FDA 510(k) K140279, S9 GREENHILLS, by Resmed, Ltd.

FDA 510(k) K140279, S9 GREENHILLS, by Resmed, Ltd.

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510(K) Number: K140279
Device Name: S9 GREENHILLS
Manufacturer: Resmed, Ltd.
Device Classification Name: Ventilator, Non-Continuous (Respirator)
Regulation Number: BZD
Classification Product Code: KXA
Date Received: 02/03/2014
Decision Date: 07/31/2014
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
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