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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
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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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.
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