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FDA 510(k)

QUIKSTRIP ONE STEP METHAMPHETAMINE

K-Number: K970395 · 1997-06-26

ApplicantDrial Consultants, Inc.
Decision Date1997-06-26
Product CodeDKZ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

QUIKSTRIP ONE STEP METHAMPHETAMINE is the device name listed in this FDA 510(k) record. The listed applicant is Drial Consultants, Inc.. It received FDA 510(k) clearance on 1997-06-26 under 510(k) number K970395. 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 QUIKSTRIP ONE STEP METHAMPHETAMINE?

QUIKSTRIP ONE STEP METHAMPHETAMINE is a medical device that received FDA 510(k) clearance on 1997-06-26. The listed applicant is Drial Consultants, Inc.. The 510(k) number is K970395.

When did QUIKSTRIP ONE STEP METHAMPHETAMINE receive FDA 510(k) clearance?

QUIKSTRIP ONE STEP METHAMPHETAMINE received FDA 510(k) clearance on 1997-06-26, under 510(k) number K970395.

Who is the listed applicant for QUIKSTRIP ONE STEP METHAMPHETAMINE?

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

What is the FDA product code for QUIKSTRIP ONE STEP METHAMPHETAMINE?

The FDA product code for QUIKSTRIP ONE STEP METHAMPHETAMINE is DKZ.

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Other records listing Drial Consultants, 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.

K973269QUIKSTRIP ONE STEP BENZODIAZEPINE TESTK973326QUIKPAC II ONE STEP BENZODIAZEPINE TESTK973047ONE STEP URINE DRUG OF ABUSE BARBITURATE TESTK972059QUIKPAC II ONE STEP COCAINE TESTK972571QUIKSTRIP ONE STEP OPIATES TESTK972405QUIKPAC II ONE STEP OPIATE TEST

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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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