FDA 510(k), K160668, HumaPen Savvio

FDA 510(k), K160668, HumaPen Savvio

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510(K) Number: K160668
Device Name: HumaPen Savvio
Manufacturer: Eli Lilly and Company, Inc.
Device Classification Name: syringe, piston
Regulation Number: 880.5860
Classification Product Code: FMF
Date Received: 03/09/2016
Decision Date: 06/03/2016
Regulation Medical Specialty: General Hospital

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