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FDA 510(k)

VERDICT-II

K-Number: K022141 · 2002-07-30

ApplicantMedtox Diagnostics, Inc.
Decision Date2002-07-30
Product CodeDJC
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

VERDICT-II is the device name listed in this FDA 510(k) record. The listed applicant is Medtox Diagnostics, Inc.. It received FDA 510(k) clearance on 2002-07-30 under 510(k) number K022141. The device is classified under product code DJC. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERDICT-II?

VERDICT-II is a medical device that received FDA 510(k) clearance on 2002-07-30. The listed applicant is Medtox Diagnostics, Inc.. The 510(k) number is K022141.

When did VERDICT-II receive FDA 510(k) clearance?

VERDICT-II received FDA 510(k) clearance on 2002-07-30, under 510(k) number K022141.

Who is the listed applicant for VERDICT-II?

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

What is the FDA product code for VERDICT-II?

The FDA product code for VERDICT-II is DJC.

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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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