LIBERTY GLUCOSE CONTROL SOLUTION
K-Number: K060481 · 2006-03-09
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Device Summary
Frequently Asked Questions
What is the LIBERTY GLUCOSE CONTROL SOLUTION?
LIBERTY GLUCOSE CONTROL SOLUTION 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 K060481.
When did LIBERTY GLUCOSE CONTROL SOLUTION receive FDA 510(k) clearance?
LIBERTY GLUCOSE CONTROL SOLUTION received FDA 510(k) clearance on 2006-03-09, under 510(k) number K060481.
Who is the listed applicant for LIBERTY GLUCOSE CONTROL SOLUTION?
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 CONTROL SOLUTION?
The FDA product code for LIBERTY GLUCOSE CONTROL SOLUTION 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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