FDA 510(k)

LIQUICHEK URINE TOXICOLOGY CONTROL (LEVEL C1)

K-Number: K050682 · 2005-04-29

Decision Date2005-04-29

Product CodeDIF

Advisory CommitteeTX

DecisionSubstantially Equivalent

Device Summary

LIQUICHEK URINE TOXICOLOGY CONTROL (LEVEL C1) 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 2005-04-29 under 510(k) number K050682. 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 (LEVEL C1)?

LIQUICHEK URINE TOXICOLOGY CONTROL (LEVEL C1) is a medical device that received FDA 510(k) clearance on 2005-04-29. The listed applicant is Bio-Rad Laboratories, Inc.. The 510(k) number is K050682.

When did LIQUICHEK URINE TOXICOLOGY CONTROL (LEVEL C1) receive FDA 510(k) clearance?

LIQUICHEK URINE TOXICOLOGY CONTROL (LEVEL C1) received FDA 510(k) clearance on 2005-04-29, under 510(k) number K050682.

Who is the listed applicant for LIQUICHEK URINE TOXICOLOGY CONTROL (LEVEL C1)?

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 (LEVEL C1)?

The FDA product code for LIQUICHEK URINE TOXICOLOGY CONTROL (LEVEL C1) is DIF.

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Related Devices (Code: DIF)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.