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FDA 510(k)

LIQUICHEK URINE TOXICOLOGY CONTROL - LEVEL S1, S2, S3

K-Number: K971691 · 1997-05-30

ApplicantBio-Rad
Decision Date1997-05-30
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

LIQUICHEK URINE TOXICOLOGY CONTROL - LEVEL S1, S2, S3 is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1997-05-30 under 510(k) number K971691. 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 S1, S2, S3?

LIQUICHEK URINE TOXICOLOGY CONTROL - LEVEL S1, S2, S3 is a medical device that received FDA 510(k) clearance on 1997-05-30. The listed applicant is Bio-Rad. The 510(k) number is K971691.

When did LIQUICHEK URINE TOXICOLOGY CONTROL - LEVEL S1, S2, S3 receive FDA 510(k) clearance?

LIQUICHEK URINE TOXICOLOGY CONTROL - LEVEL S1, S2, S3 received FDA 510(k) clearance on 1997-05-30, under 510(k) number K971691.

Who is the listed applicant for LIQUICHEK URINE TOXICOLOGY CONTROL - LEVEL S1, S2, S3?

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

What is the FDA product code for LIQUICHEK URINE TOXICOLOGY CONTROL - LEVEL S1, S2, S3?

The FDA product code for LIQUICHEK URINE TOXICOLOGY CONTROL - LEVEL S1, S2, S3 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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