FDA 510(k), K142518, HumaPen Luxura

FDA 510(k), K142518, HumaPen Luxura

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510(K) Number: K142518
Device Name: HumaPen Luxura
Manufacturer: ELI LILLY AND COMPANY
Device Classification Name: syringe, piston
Regulation Number: 880.5860
Classification Product Code: FMF
Date Received: 09/08/2014
Decision Date: 06/05/2015
Regulation Medical Specialty: General Hospital

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