LIBERTY GLUCOSE NORMAL CONTROL SOLUTIONS, MODEL 2120041
K-Number: K060426 · 2006-03-09
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Device Summary
Frequently Asked Questions
What is the LIBERTY GLUCOSE NORMAL CONTROL SOLUTIONS, MODEL 2120041?
LIBERTY GLUCOSE NORMAL CONTROL SOLUTIONS, MODEL 2120041 is a medical device that received FDA 510(k) clearance on 2006-03-09. The listed applicant is Liberty Healthcare Group, Inc.. The 510(k) number is K060426.
When did LIBERTY GLUCOSE NORMAL CONTROL SOLUTIONS, MODEL 2120041 receive FDA 510(k) clearance?
LIBERTY GLUCOSE NORMAL CONTROL SOLUTIONS, MODEL 2120041 received FDA 510(k) clearance on 2006-03-09, under 510(k) number K060426.
Who is the listed applicant for LIBERTY GLUCOSE NORMAL CONTROL SOLUTIONS, MODEL 2120041?
The FDA 510(k) record lists Liberty Healthcare Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIBERTY GLUCOSE NORMAL CONTROL SOLUTIONS, MODEL 2120041?
The FDA product code for LIBERTY GLUCOSE NORMAL CONTROL SOLUTIONS, MODEL 2120041 is JJX.
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 Liberty Healthcare Group, 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: JJX)
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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