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FDA 510(k)

UCP MULTIPLE DRUG SCREEN TEST CUPS

K-Number: K072062 · 2007-09-20

ApplicantUcp Biosciences, Inc.
Decision Date2007-09-20
Product CodeLFG
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

UCP MULTIPLE DRUG SCREEN TEST CUPS is the device name listed in this FDA 510(k) record. The listed applicant is Ucp Biosciences, Inc.. It received FDA 510(k) clearance on 2007-09-20 under 510(k) number K072062. The device is classified under product code LFG. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UCP MULTIPLE DRUG SCREEN TEST CUPS?

UCP MULTIPLE DRUG SCREEN TEST CUPS is a medical device that received FDA 510(k) clearance on 2007-09-20. The listed applicant is Ucp Biosciences, Inc.. The 510(k) number is K072062.

When did UCP MULTIPLE DRUG SCREEN TEST CUPS receive FDA 510(k) clearance?

UCP MULTIPLE DRUG SCREEN TEST CUPS received FDA 510(k) clearance on 2007-09-20, under 510(k) number K072062.

Who is the listed applicant for UCP MULTIPLE DRUG SCREEN TEST CUPS?

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

What is the FDA product code for UCP MULTIPLE DRUG SCREEN TEST CUPS?

The FDA product code for UCP MULTIPLE DRUG SCREEN TEST CUPS is LFG.

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Other records listing Ucp Biosciences, 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.

K152908UCP COMPACT DRUG TESTSK131236UCP PREGNANCY CASSETTE TEST, DIP/CARD STRIP, HOME PREGNANCY CASSETTE TEST, MIDSTREAM TEST AND DIP/CARD STRIPK131811UCP COMPACT DRUG TEST CARDS, UCP COMPACT DRUG TEST CUPSK130463UCP HOME DRUG SCREENING TEST; CARDS, CUPSK123863UCP COMPACT DRUG TEST CARDS, UCP COMPACT DRUG TEST CUPSK122419UCP HOME DRUG SCREENING TEST CUPS

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Related Devices (Code: LFG)

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.

K112395WONDFO PHENCYCLIDINE URINE TEST, TRICYCLIC ANTIDEPRESSANTS URINE TESTGuangzhou Wondfo Biotech Co., Ltd.K061457UCP RAPID DRUG SCREENING TRICYCLIC ANTIDEPRESSANT, PROPOXYPHENE TESTSUcp Biosciences, Inc.K021526ACON TCA ONE STEP TRICYCLIC ANTIDEPRESSANT TEST STRIP AND DEVICEACON Laboratories, Inc.K011545VERDICT -II TCA, VERDICT-II MTDMedtox Diagnostics, Inc.K980249ACCUSIGN TCA, BIOSIGN TCA, STAUS DS TCAPrinceton BioMeditech Corp.K870823EMIT NORTRIPTYLINE ASSAYSyva Co.

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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