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FDA 510(k)

LIVESURE BARBITURATES SCREEN TEST

K-Number: K012133 · 2001-07-20

ApplicantPan Probe Biotech, Inc.
Decision Date2001-07-20
Product CodeDIS
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

LIVESURE BARBITURATES SCREEN TEST is the device name listed in this FDA 510(k) record. The listed applicant is Pan Probe Biotech, Inc.. It received FDA 510(k) clearance on 2001-07-20 under 510(k) number K012133. The device is classified under product code DIS. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIVESURE BARBITURATES SCREEN TEST?

LIVESURE BARBITURATES SCREEN TEST is a medical device that received FDA 510(k) clearance on 2001-07-20. The listed applicant is Pan Probe Biotech, Inc.. The 510(k) number is K012133.

When did LIVESURE BARBITURATES SCREEN TEST receive FDA 510(k) clearance?

LIVESURE BARBITURATES SCREEN TEST received FDA 510(k) clearance on 2001-07-20, under 510(k) number K012133.

Who is the listed applicant for LIVESURE BARBITURATES SCREEN TEST?

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

What is the FDA product code for LIVESURE BARBITURATES SCREEN TEST?

The FDA product code for LIVESURE BARBITURATES SCREEN TEST is DIS.

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Other records listing Pan Probe Biotech, 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.

K020968LIVESURE HCG URINARY PREGNANCY TEST STRIP AND TEST CARDK013796LIVESURE METHADONE SCREEN TESTSK012107LIVESURE PHENECYCLINE (PCP) SCREEN TESTSK012131LIVESURE BENZODIAZEPINES SCREEN TESTSK011610LIVESURE METHAMPHETAMINE SCREEN TESTSK011609LIVESURE AMPHETAMINE SCREEN TEST

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Related Devices (Code: DIS)

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.

K161714Immunalysis Barbiturates Urine Enzyme Immunoassay, Immunalysis Multi-Drug CalibratorsImmunalysis CorporationK092268RANDOX BARITURATES ASSAYRandox Laboratories, Ltd.K110515UCP DRUG SCREENING TEST CUPSUcp Biosciences, Inc.K070098QUICKSCREEN BARBITURATE 300 SCREENING TEST, MODELS 9019, 9018; MULTI DRUG SCREENING TEST, MODEL 9317T; CUP MULTI DRUG SCPhamatech, Inc.K070009AT HOME DRUG TEST MODELS, 9308T AND 9308XPhamatech, Inc.K062165VITROS CHEMISTRY PRODUCTS BARB REAGENT; CALIBRATOR KIT 26; FS CALIBRATOR 1; DAT PERFORMANCE VERIFIERSOrtho-Clinical Diagnostics

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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