FDA 510(k), K053563, HUMAPEN MEMOIR

FDA 510(k), K053563, HUMAPEN MEMOIR

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510(K) Number: K053563
Device Name: HUMAPEN MEMOIR
Manufacturer: ELI LILLY AND COMPANY
Device Classification Name: syringe, piston
Regulation Number: 880.5860
Classification Product Code: FMF
Date Received: 12/21/2005
Decision Date: 04/07/2006
Regulation Medical Specialty: General Hospital

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