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FDA 510(k)

CHOLESTRAK HDL CHOLESTEROL HOME TEST

K-Number: K072836 · 2007-12-27

ApplicantAccutech, LLC
Decision Date2007-12-27
Product CodeLBS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CHOLESTRAK HDL CHOLESTEROL HOME TEST is the device name listed in this FDA 510(k) record. The listed applicant is Accutech, LLC. It received FDA 510(k) clearance on 2007-12-27 under 510(k) number K072836. The device is classified under product code LBS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHOLESTRAK HDL CHOLESTEROL HOME TEST?

CHOLESTRAK HDL CHOLESTEROL HOME TEST is a medical device that received FDA 510(k) clearance on 2007-12-27. The listed applicant is Accutech, LLC. The 510(k) number is K072836.

When did CHOLESTRAK HDL CHOLESTEROL HOME TEST receive FDA 510(k) clearance?

CHOLESTRAK HDL CHOLESTEROL HOME TEST received FDA 510(k) clearance on 2007-12-27, under 510(k) number K072836.

Who is the listed applicant for CHOLESTRAK HDL CHOLESTEROL HOME TEST?

The FDA 510(k) record lists Accutech, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHOLESTRAK HDL CHOLESTEROL HOME TEST?

The FDA product code for CHOLESTRAK HDL CHOLESTEROL HOME TEST is LBS.

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.

Related Devices (Code: LBS)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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