CHOLESTAT (TM) WHOLE BLOOD CHOLESTEROL TEST
K-Number: K910240 · 1991-02-26
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Device Summary
Frequently Asked Questions
What is the CHOLESTAT (TM) WHOLE BLOOD CHOLESTEROL TEST?
CHOLESTAT (TM) WHOLE BLOOD CHOLESTEROL TEST is a medical device that received FDA 510(k) clearance on 1991-02-26. The listed applicant is Crystal Diagnostics, Inc.. The 510(k) number is K910240.
When did CHOLESTAT (TM) WHOLE BLOOD CHOLESTEROL TEST receive FDA 510(k) clearance?
CHOLESTAT (TM) WHOLE BLOOD CHOLESTEROL TEST received FDA 510(k) clearance on 1991-02-26, under 510(k) number K910240.
Who is the listed applicant for CHOLESTAT (TM) WHOLE BLOOD CHOLESTEROL TEST?
The FDA 510(k) record lists Crystal Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHOLESTAT (TM) WHOLE BLOOD CHOLESTEROL TEST?
The FDA product code for CHOLESTAT (TM) WHOLE BLOOD CHOLESTEROL TEST is CHH.
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 Crystal 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: CHH)
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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