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FDA 510(k)

FINGERPRINT DRUG SCREENING DEVICE

K-Number: K973726 · 1997-11-06

ApplicantApplied Technology Ventures, LLC
Decision Date1997-11-06
Product CodeDKZ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

FINGERPRINT DRUG SCREENING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Applied Technology Ventures, LLC. It received FDA 510(k) clearance on 1997-11-06 under 510(k) number K973726. 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 FINGERPRINT DRUG SCREENING DEVICE?

FINGERPRINT DRUG SCREENING DEVICE is a medical device that received FDA 510(k) clearance on 1997-11-06. The listed applicant is Applied Technology Ventures, LLC. The 510(k) number is K973726.

When did FINGERPRINT DRUG SCREENING DEVICE receive FDA 510(k) clearance?

FINGERPRINT DRUG SCREENING DEVICE received FDA 510(k) clearance on 1997-11-06, under 510(k) number K973726.

Who is the listed applicant for FINGERPRINT DRUG SCREENING DEVICE?

The FDA 510(k) record lists Applied Technology Ventures, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FINGERPRINT DRUG SCREENING DEVICE?

The FDA product code for FINGERPRINT DRUG SCREENING DEVICE is DKZ.

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.

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Other records listing Applied Technology Ventures, LLC 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.

K980836GENIE CUP INTEGRATED SCREENING DEVICE

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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