FDA 510(k), K202037, imani i2

FDA 510(k), K202037, imani i2

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510(K) Number: K202037
Device Name: imani i2
Manufacturer: imani Co.
Device Classification Name: pump, breast, powered
Regulation Number: 884.5160
Classification Product Code: HGX
Date Received: 07/23/2020
Decision Date: 03/01/2021
Regulation Medical Specialty: Obstetrics/Gynecology

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