FDA 510(k), K111411, FREEMIE (R)

FDA 510(k), K111411, FREEMIE (R)

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510(K) Number: K111411
Device Name: FREEMIE (R)
Manufacturer: DAO HEALTH
Device Classification Name: Pump, Breast, Powered
Regulation Number: 884.5160
Classification Product Code: HGX
Date Received: 05/20/2011
Decision Date: 02/01/2012
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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