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
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
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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