FDA 510(k)

USDT CANNABINOID (THC) ASSAY COLUMN CATALOG NO. 9000-500

K-Number: K940912 · 1994-06-02

Decision Date1994-06-02

Product CodeLDJ

Advisory CommitteeTX

DecisionSubstantially Equivalent

Device Summary

USDT CANNABINOID (THC) ASSAY COLUMN CATALOG NO. 9000-500 is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Drug Testing, Inc.. It received FDA 510(k) clearance on 1994-06-02 under 510(k) number K940912. The device is classified under product code LDJ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the USDT CANNABINOID (THC) ASSAY COLUMN CATALOG NO. 9000-500?

USDT CANNABINOID (THC) ASSAY COLUMN CATALOG NO. 9000-500 is a medical device that received FDA 510(k) clearance on 1994-06-02. The listed applicant is U.S. Drug Testing, Inc.. The 510(k) number is K940912.

When did USDT CANNABINOID (THC) ASSAY COLUMN CATALOG NO. 9000-500 receive FDA 510(k) clearance?

USDT CANNABINOID (THC) ASSAY COLUMN CATALOG NO. 9000-500 received FDA 510(k) clearance on 1994-06-02, under 510(k) number K940912.

Who is the listed applicant for USDT CANNABINOID (THC) ASSAY COLUMN CATALOG NO. 9000-500?

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

What is the FDA product code for USDT CANNABINOID (THC) ASSAY COLUMN CATALOG NO. 9000-500?

The FDA product code for USDT CANNABINOID (THC) ASSAY COLUMN CATALOG NO. 9000-500 is LDJ.

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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.