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FDA 510(k)

LIQUICHEK URINE TOXICOLOGY CONTROL (SCREEN SERIES)

K-Number: K033924 · 2004-02-03

ApplicantBio-Rad Laboratories, Inc.
Decision Date2004-02-03
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

LIQUICHEK URINE TOXICOLOGY CONTROL (SCREEN SERIES) is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad Laboratories, Inc.. It received FDA 510(k) clearance on 2004-02-03 under 510(k) number K033924. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUICHEK URINE TOXICOLOGY CONTROL (SCREEN SERIES)?

LIQUICHEK URINE TOXICOLOGY CONTROL (SCREEN SERIES) is a medical device that received FDA 510(k) clearance on 2004-02-03. The listed applicant is Bio-Rad Laboratories, Inc.. The 510(k) number is K033924.

When did LIQUICHEK URINE TOXICOLOGY CONTROL (SCREEN SERIES) receive FDA 510(k) clearance?

LIQUICHEK URINE TOXICOLOGY CONTROL (SCREEN SERIES) received FDA 510(k) clearance on 2004-02-03, under 510(k) number K033924.

Who is the listed applicant for LIQUICHEK URINE TOXICOLOGY CONTROL (SCREEN SERIES)?

The FDA 510(k) record lists Bio-Rad Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIQUICHEK URINE TOXICOLOGY CONTROL (SCREEN SERIES)?

The FDA product code for LIQUICHEK URINE TOXICOLOGY CONTROL (SCREEN SERIES) is DIF.

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Related Devices (Code: DIF)

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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