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FDA 510(k)

USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200

K-Number: K932318 · 1993-06-15

Decision Date1993-06-15
Product CodeDJG
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200 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 1993-06-15 under 510(k) number K932318. 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 USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200?

USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200 is a medical device that received FDA 510(k) clearance on 1993-06-15. The listed applicant is U.S. Drug Testing, Inc.. The 510(k) number is K932318.

When did USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200 receive FDA 510(k) clearance?

USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200 received FDA 510(k) clearance on 1993-06-15, under 510(k) number K932318.

Who is the listed applicant for USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200?

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 OPIATE ASSAY COLUMN CATALOG NO. 9000-200?

The FDA product code for USDT OPIATE ASSAY COLUMN CATALOG NO. 9000-200 is DJG.

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.

Other records listing U.S. Drug Testing, Inc. as applicant

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: DJG)

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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