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FDA 510(k)

HUMAPEN LUXURA HD

K-Number: K063151 · 2007-01-09

ApplicantEli Lilly and Co.
Decision Date2007-01-09
Product CodeNSC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HUMAPEN LUXURA HD is the device name listed in this FDA 510(k) record. The listed applicant is Eli Lilly and Co.. It received FDA 510(k) clearance on 2007-01-09 under 510(k) number K063151. The device is classified under product code NSC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUMAPEN LUXURA HD?

HUMAPEN LUXURA HD is a medical device that received FDA 510(k) clearance on 2007-01-09. The listed applicant is Eli Lilly and Co.. The 510(k) number is K063151.

When did HUMAPEN LUXURA HD receive FDA 510(k) clearance?

HUMAPEN LUXURA HD received FDA 510(k) clearance on 2007-01-09, under 510(k) number K063151.

Who is the listed applicant for HUMAPEN LUXURA HD?

The FDA 510(k) record lists Eli Lilly and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HUMAPEN LUXURA HD?

The FDA product code for HUMAPEN LUXURA HD is NSC.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Eli Lilly and Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K982842HUMAPEN AND HUMAPEN ERGO

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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