LIFEGLOBAL HUMAN SERUM ALBUMIN LG HSA
K-Number: K083509 · 2009-04-24
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Device Summary
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.
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
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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