FDA 510(k), K190292, Passio Pump Drainage System

FDA 510(k), K190292, Passio Pump Drainage System

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510(K) Number: K190292
Device Name: Passio Pump Drainage System
Manufacturer: Bearpac Medical
Device Classification Name: Apparatus, Suction, Patient Care
Regulation Number: 870.5050
Classification Product Code: DWM
Date Received: 02/11/2019
Decision Date: 07/25/2019
Regulation Medical Specialty: Cardiovascular

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