FDA 510(k), K182749, Lansinoh Signature Pro Double Electric Breast Pump, Lansinoh Smartpump Double Electric Breast Pump

FDA 510(k), K182749, Lansinoh Signature Pro Double Electric Breast Pump, Lansinoh Smartpump Double Electric Breast Pump

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510(K) Number: K182749
Device Name: Lansinoh Signature Pro Double Electric Breast Pump, Lansinoh Smartpump Double Electric Breast Pump
Manufacturer: Lansinoh Laboratories Saglik Gerecleri Tasarim San. Tic. Ltd
Device Classification Name: pump, breast, powered
Regulation Number: 884.5160
Classification Product Code: HGX
Date Received: 09/28/2018
Decision Date: 06/12/2019
Regulation Medical Specialty: Obstetrics/Gynecology

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