FDA 510(k), K172772, Freemie Independence, Freemie Liberty

FDA 510(k), K172772, Freemie Independence, Freemie Liberty

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510(K) Number: K172772
Device Name: Freemie Independence, Freemie Liberty
Manufacturer: DAO Health
Device Classification Name: Pump, Breast, Powered
Regulation Number: 884.5160
Classification Product Code: HGX
Date Received: 09/14/2017
Decision Date: 10/13/2017
Regulation Medical Specialty: Obstetrics/Gynecology

NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.

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