FDA 510(k), K130702, AIRSONETT AIR-4

FDA 510(k), K130702, AIRSONETT AIR-4

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510(K) Number: K130702
Device Name: AIRSONETT AIR-4
Manufacturer:
Device Classification Name: Cleaner, Air, Medical Recirculating
Regulation Number: 880.5045
Classification Product Code: FRF
Date Received: 03/15/2013
Decision Date: 07/23/2013
Regulation Medical Specialty: General Hospital
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