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FDA 510(k)

MICROLINE SCREEN FOR CANNABINOID

K-Number: K914915 · 1992-01-22

ApplicantDrug Screening Systems, Inc.
Decision Date1992-01-22
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

MICROLINE SCREEN FOR CANNABINOID is the device name listed in this FDA 510(k) record. The listed applicant is Drug Screening Systems, Inc.. It received FDA 510(k) clearance on 1992-01-22 under 510(k) number K914915. 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 MICROLINE SCREEN FOR CANNABINOID?

MICROLINE SCREEN FOR CANNABINOID is a medical device that received FDA 510(k) clearance on 1992-01-22. The listed applicant is Drug Screening Systems, Inc.. The 510(k) number is K914915.

When did MICROLINE SCREEN FOR CANNABINOID receive FDA 510(k) clearance?

MICROLINE SCREEN FOR CANNABINOID received FDA 510(k) clearance on 1992-01-22, under 510(k) number K914915.

Who is the listed applicant for MICROLINE SCREEN FOR CANNABINOID?

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

What is the FDA product code for MICROLINE SCREEN FOR CANNABINOID?

The FDA product code for MICROLINE SCREEN FOR CANNABINOID is LDJ.

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Other records listing Drug Screening Systems, 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.

K945829MICROLINE SCREEN FOR BENZODIAZEPINEK935052MICROLINE SCREEN FOR AMPHETAMINEK933480MICROLINE SCREEN FOR BARBITURATESK921651MICROLINE SCREEN FOR PHENCYCLIDINEK911652MIRCOLINE SCREEN FOR COCAINEK910525MICROLINE SCREEN FOR METHAMPHETAMINE

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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.

K232732Rapid Marijuana (THC) Test Strip 20, Rapid Marijuana (THC) Test Dipcard 20, Rapid Marijuana (THC) Test Strip 50, Rapid Marijuana (THC) Test Dipcard 50Co-Innovation Biotech Co., Ltd.K232604LYHER® Urine Marijuana (THC) Test Kit (Strip), LYHER® Urine Marijuana (THC) Test Kit (Cassette)Hangzhou Laihe Biotech Co., Ltd.K223162Healgen® Accurate Oral Fluid Drug Test, Healgen® Accurate Oral Fluid Drug Test COTHealgen Scientific,, LLCK192515BIOEASY Marijuana Test Dip Card 40, BIOEASY Marijuana Test Dip Card 20, BIOEASY Marijuana Test Strip 40, BIOEASY Marijuana Test Strip 20Shenzhen Bioeasy Biotechnology Co., Ltd.K153741CLUNGENE Methamphetamine Test, CLUNGENE Morphine Test, CLUNGENE Marijuana TestHangzhou Clongene Biotech Co., Ltd.K130213QUICKPROFILE SINGLE DRUG OF ABUSE DEVICE AND QUICK PROFILE MULTI-DRUGS OF ABUSE SCREEN DEVICELumiquick Diagnostics, Inc.

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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