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FDA 510(k)

LIVESURE BENZODIAZEPINES SCREEN TESTS

K-Number: K012131 · 2001-07-20

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

Device Summary

LIVESURE BENZODIAZEPINES SCREEN TESTS 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 K012131. The device is classified under product code JXM. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIVESURE BENZODIAZEPINES SCREEN TESTS?

LIVESURE BENZODIAZEPINES SCREEN TESTS 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 K012131.

When did LIVESURE BENZODIAZEPINES SCREEN TESTS receive FDA 510(k) clearance?

LIVESURE BENZODIAZEPINES SCREEN TESTS received FDA 510(k) clearance on 2001-07-20, under 510(k) number K012131.

Who is the listed applicant for LIVESURE BENZODIAZEPINES SCREEN TESTS?

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 BENZODIAZEPINES SCREEN TESTS?

The FDA product code for LIVESURE BENZODIAZEPINES SCREEN TESTS is JXM.

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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 TESTSK012133LIVESURE BARBITURATES SCREEN TESTK012107LIVESURE PHENECYCLINE (PCP) SCREEN TESTSK011610LIVESURE METHAMPHETAMINE SCREEN TESTSK011609LIVESURE AMPHETAMINE SCREEN TEST

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Related Devices (Code: JXM)

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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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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