GLUCOCHEK POCKETLAB
K-Number: K951457 · 1996-02-22
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Device Summary
Frequently Asked Questions
What is the GLUCOCHEK POCKETLAB?
GLUCOCHEK POCKETLAB is a medical device that received FDA 510(k) clearance on 1996-02-22. The listed applicant is Clinical Diagnostics, Inc.. The 510(k) number is K951457.
When did GLUCOCHEK POCKETLAB receive FDA 510(k) clearance?
GLUCOCHEK POCKETLAB received FDA 510(k) clearance on 1996-02-22, under 510(k) number K951457.
Who is the listed applicant for GLUCOCHEK POCKETLAB?
The FDA 510(k) record lists Clinical Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GLUCOCHEK POCKETLAB?
The FDA product code for GLUCOCHEK POCKETLAB is CGA.
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 Clinical Diagnostics, 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: CGA)
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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