FDA 510(k), K130524, BREATHID HP SYSTEM

FDA 510(k), K130524, BREATHID HP SYSTEM

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510(K) Number: K130524
Device Name: BREATHID HP SYSTEM
Manufacturer:
Device Classification Name: Test, Urea (Breath Or Blood)
Regulation Number: 866.3110
Classification Product Code: MSQ
Date Received: 02/28/2013
Decision Date: 05/22/2013
Regulation Medical Specialty: Microbiology
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