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FDA 510(k)

SCREENERS MARIJUANA TEST, DRUGSCREEN DIP MARIJUANA TEST

K-Number: K992949 · 1999-12-27

Decision Date1999-12-27
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

SCREENERS MARIJUANA TEST, DRUGSCREEN DIP MARIJUANA TEST is the device name listed in this FDA 510(k) record. The listed applicant is Drug Detection Devices, Ltd.. It received FDA 510(k) clearance on 1999-12-27 under 510(k) number K992949. 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 SCREENERS MARIJUANA TEST, DRUGSCREEN DIP MARIJUANA TEST?

SCREENERS MARIJUANA TEST, DRUGSCREEN DIP MARIJUANA TEST is a medical device that received FDA 510(k) clearance on 1999-12-27. The listed applicant is Drug Detection Devices, Ltd.. The 510(k) number is K992949.

When did SCREENERS MARIJUANA TEST, DRUGSCREEN DIP MARIJUANA TEST receive FDA 510(k) clearance?

SCREENERS MARIJUANA TEST, DRUGSCREEN DIP MARIJUANA TEST received FDA 510(k) clearance on 1999-12-27, under 510(k) number K992949.

Who is the listed applicant for SCREENERS MARIJUANA TEST, DRUGSCREEN DIP MARIJUANA TEST?

The FDA 510(k) record lists Drug Detection Devices, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCREENERS MARIJUANA TEST, DRUGSCREEN DIP MARIJUANA TEST?

The FDA product code for SCREENERS MARIJUANA TEST, DRUGSCREEN DIP MARIJUANA TEST is LDJ.

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 Drug Detection Devices, Ltd. 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.

View all 8 devices →

Related Devices (Code: LDJ)

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

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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