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FDA 510(k)

LIQUI-URA TOXIC URINE CONTROL

K-Number: K834259 · 1984-01-30

Decision Date1984-01-30
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

LIQUI-URA TOXIC URINE CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Biodiagnostic Intl. It received FDA 510(k) clearance on 1984-01-30 under 510(k) number K834259. 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 LIQUI-URA TOXIC URINE CONTROL?

LIQUI-URA TOXIC URINE CONTROL is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is Biodiagnostic Intl. The 510(k) number is K834259.

When did LIQUI-URA TOXIC URINE CONTROL receive FDA 510(k) clearance?

LIQUI-URA TOXIC URINE CONTROL received FDA 510(k) clearance on 1984-01-30, under 510(k) number K834259.

Who is the listed applicant for LIQUI-URA TOXIC URINE CONTROL?

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

What is the FDA product code for LIQUI-URA TOXIC URINE CONTROL?

The FDA product code for LIQUI-URA TOXIC URINE CONTROL is DIF.

Related Clinical Trials

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.

Other records listing Biodiagnostic Intl 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.

View all 11 devices →

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.

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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