FDA 510(k), K181372, Argos

FDA 510(k), K181372, Argos

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510(K) Number: K181372
Device Name: Argos
Manufacturer: Retia Medical, LLC
Device Classification Name: Computer, Diagnostic, Pre-Programmed, Single-Function
Regulation Number: 870.1435
Classification Product Code: DXG
Date Received: 05/23/2018
Decision Date: 12/13/2018
Regulation Medical Specialty: Cardiovascular

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