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FDA 510(k)

LIFEGLOBAL HUMAN SERUM ALBUMIN LG HSA

K-Number: K083509 · 2009-04-24

Decision Date2009-04-24
Product CodeMQL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LIFEGLOBAL HUMAN SERUM ALBUMIN LG HSA is the device name listed in this FDA 510(k) record. The listed applicant is Genx Intl., Inc.. It received FDA 510(k) clearance on 2009-04-24 under 510(k) number K083509. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFEGLOBAL HUMAN SERUM ALBUMIN LG HSA?

LIFEGLOBAL HUMAN SERUM ALBUMIN LG HSA is a medical device that received FDA 510(k) clearance on 2009-04-24. The listed applicant is Genx Intl., Inc.. The 510(k) number is K083509.

When did LIFEGLOBAL HUMAN SERUM ALBUMIN LG HSA receive FDA 510(k) clearance?

LIFEGLOBAL HUMAN SERUM ALBUMIN LG HSA received FDA 510(k) clearance on 2009-04-24, under 510(k) number K083509.

Who is the listed applicant for LIFEGLOBAL HUMAN SERUM ALBUMIN LG HSA?

The FDA 510(k) record lists Genx Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFEGLOBAL HUMAN SERUM ALBUMIN LG HSA?

The FDA product code for LIFEGLOBAL HUMAN SERUM ALBUMIN LG HSA is MQL.

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.

Other records listing Genx Intl., Inc. 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.

View all 32 devices →

Related Devices (Code: MQL)

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.

Official Source

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

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