FDA 510(k), K130304, LMA FAMILY OF AIRWAYS

FDA 510(k), K130304, LMA FAMILY OF AIRWAYS

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510(K) Number: K130304
Device Name: LMA FAMILY OF AIRWAYS
Manufacturer: THE LARYNGEAL MASK CO.,LTD.
Device Classification Name: Airway, Oropharyngeal, Anesthesiology
Regulation Number: 868.5110
Classification Product Code: CAE
Date Received: 02/07/2013
Decision Date: 05/30/2014
Regulation Medical Specialty: Anesthesiology
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