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FDA 510(k), K142518, HumaPen Luxura
FDA 510(k), K142518, HumaPen Luxura
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$89.00 USD
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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
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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- 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. Learn more about Fast-Track Requests here.
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