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FDA 510(k)

STARTOX DRUG OF ABUSE SCREENING TEST

K-Number: K021006 · 2002-06-10

ApplicantStarplex Scientific, Inc.
Decision Date2002-06-10
Product CodeDKZ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

STARTOX DRUG OF ABUSE SCREENING TEST is the device name listed in this FDA 510(k) record. The listed applicant is Starplex Scientific, Inc.. It received FDA 510(k) clearance on 2002-06-10 under 510(k) number K021006. The device is classified under product code DKZ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STARTOX DRUG OF ABUSE SCREENING TEST?

STARTOX DRUG OF ABUSE SCREENING TEST is a medical device that received FDA 510(k) clearance on 2002-06-10. The listed applicant is Starplex Scientific, Inc.. The 510(k) number is K021006.

When did STARTOX DRUG OF ABUSE SCREENING TEST receive FDA 510(k) clearance?

STARTOX DRUG OF ABUSE SCREENING TEST received FDA 510(k) clearance on 2002-06-10, under 510(k) number K021006.

Who is the listed applicant for STARTOX DRUG OF ABUSE SCREENING TEST?

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

What is the FDA product code for STARTOX DRUG OF ABUSE SCREENING TEST?

The FDA product code for STARTOX DRUG OF ABUSE SCREENING TEST is DKZ.

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Other records listing Starplex Scientific, 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.

K032246MODIFICATION TO MULTITRANS CULTURE COLLECTION AND TRANSPORT SYSTEMK022388STARTOX DRUG OF ABUSE SCREENING TEST (4)K962843MULTITRANS CULTURE COLLECTION AND TRANSPORT SYSTEMK960997STARSWAB CULTURE COLLECTION AND TRANSPORT SYSTEMK944847KULTSURE/STARSWAB ANAEROBIC TRANSPORT SYSTEMK924364VACUPLUS TUBES WITH GREY STOPPERS

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Related Devices (Code: DKZ)

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.

K240670DRI Ecstasy Plus AssayMicrogenics CorporationK233019AllTest Multi-Drug Rapid Test Cup; AllTest Multi-Drug Rapid Test Panel; AllTest Multi-Drug Rapid Test Cup Rx; AllTest Multi-Drug Rapid Test Panel RxHangzhou AllTest Biotech Co., Ltd.K231137Xenta Drug Screen Cup, Xenta Drug Screen DipcardXenta Biomedical Science Co., Ltd.K200363Quidel Triage® TOX Drug Screen, 94600Quidel Cardiovascular, Inc.K191099Atlas Multi-Drugs Screening Test Cup, Atlas Multi-Drugs Screening Test PanelAtlas MedicalK182719Quidel Triage TOX Drug Screen, 94600; Quidel Triage® MeterProQuidel Cardiovascular, 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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