FDA 510(k), K142541, POCKET NEB

FDA 510(k), K142541, POCKET NEB

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510(K) Number: K142541
Device Name: POCKET NEB
Manufacturer: MicroVaper Devices
Device Classification Name: nebulizer (direct patient interface)
Regulation Number: 868.5630
Classification Product Code: CAF
Date Received: 09/10/2014
Decision Date: 01/22/2016
Regulation Medical Specialty: Anesthesiology

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