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FDA 510(k)

VAP-NT CHOLESTEROL TEST

K-Number: K062026 · 2007-03-06

Decision Date2007-03-06
Product CodeCHH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VAP-NT CHOLESTEROL TEST is the device name listed in this FDA 510(k) record. The listed applicant is Atherotech, Inc.. It received FDA 510(k) clearance on 2007-03-06 under 510(k) number K062026. The device is classified under product code CHH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAP-NT CHOLESTEROL TEST?

VAP-NT CHOLESTEROL TEST is a medical device that received FDA 510(k) clearance on 2007-03-06. The listed applicant is Atherotech, Inc.. The 510(k) number is K062026.

When did VAP-NT CHOLESTEROL TEST receive FDA 510(k) clearance?

VAP-NT CHOLESTEROL TEST received FDA 510(k) clearance on 2007-03-06, under 510(k) number K062026.

Who is the listed applicant for VAP-NT CHOLESTEROL TEST?

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

What is the FDA product code for VAP-NT CHOLESTEROL TEST?

The FDA product code for VAP-NT 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.

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

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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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