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FDA 510(k)

VERDICT -II OPIATES 2000

K-Number: K992111 · 1999-12-16

ApplicantMedtox Diagnostics, Inc.
Decision Date1999-12-16
Product CodeDJG
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

VERDICT -II OPIATES 2000 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 1999-12-16 under 510(k) number K992111. The device is classified under product code DJG. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERDICT -II OPIATES 2000?

VERDICT -II OPIATES 2000 is a medical device that received FDA 510(k) clearance on 1999-12-16. The listed applicant is Medtox Diagnostics, Inc.. The 510(k) number is K992111.

When did VERDICT -II OPIATES 2000 receive FDA 510(k) clearance?

VERDICT -II OPIATES 2000 received FDA 510(k) clearance on 1999-12-16, under 510(k) number K992111.

Who is the listed applicant for VERDICT -II OPIATES 2000?

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 OPIATES 2000?

The FDA product code for VERDICT -II OPIATES 2000 is DJG.

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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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