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FDA 510(k)

QUIKSTRIP DIPSCAN X MULTIDRUG SCREENING DEVICE

K-Number: K990325 · 1999-06-24

ApplicantSyntron Bioresearch, Inc.
Decision Date1999-06-24
Product CodeDKZ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

QUIKSTRIP DIPSCAN X MULTIDRUG SCREENING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Syntron Bioresearch, Inc.. It received FDA 510(k) clearance on 1999-06-24 under 510(k) number K990325. 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 DIPSCAN X MULTIDRUG SCREENING DEVICE?

QUIKSTRIP DIPSCAN X MULTIDRUG SCREENING DEVICE is a medical device that received FDA 510(k) clearance on 1999-06-24. The listed applicant is Syntron Bioresearch, Inc.. The 510(k) number is K990325.

When did QUIKSTRIP DIPSCAN X MULTIDRUG SCREENING DEVICE receive FDA 510(k) clearance?

QUIKSTRIP DIPSCAN X MULTIDRUG SCREENING DEVICE received FDA 510(k) clearance on 1999-06-24, under 510(k) number K990325.

Who is the listed applicant for QUIKSTRIP DIPSCAN X MULTIDRUG SCREENING DEVICE?

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

What is the FDA product code for QUIKSTRIP DIPSCAN X MULTIDRUG SCREENING DEVICE?

The FDA product code for QUIKSTRIP DIPSCAN X MULTIDRUG SCREENING DEVICE is DKZ.

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Other records listing Syntron Bioresearch, 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.

K993490QUICKSTRIP ONE STEP OPIATES TESTK993491QUICKPAC II ONE STEP OPIATES TESTK992990QUICKPAC II ONE STEP COCAINE TESTK992748DRUGCHECK X MULTIDRUG SCREENING DEVICEK992207QUIKSTRIP ONE STEP COCAINE ASSAY (COCAINE AND COCAINE METABOLITE TEST SYSTEMK983113BESURE PLUS ONE-STEP HOME OVULATION PREDICTOR KIT

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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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