HUMAPEN LUXURA HD— 510(k) K063151

Substantially Equivalent

Eli Lilly and Co.

FDA 510(k) clearance K063151 for HUMAPEN LUXURA HD, Substantially Equivalent on 2007-01-09. Applicant: Eli Lilly and Co..

Clearance details

Applicant: Eli Lilly and Co.
Product code: Code NSC
Advisory panel: General Hospital
Date received: 2006-10-16
Decision date: 2007-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

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