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FDA 510(k)

CANNABINOID URINE DRUGS OF ABUSE CALIBRATORS AND CONTROLS

K-Number: K021449 · 2002-06-18

Decision Date2002-06-18
Product CodeDLJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

CANNABINOID URINE DRUGS OF ABUSE CALIBRATORS AND CONTROLS is the device name listed in this FDA 510(k) record. The listed applicant is Lin-Zhi International, Inc.. It received FDA 510(k) clearance on 2002-06-18 under 510(k) number K021449. The device is classified under product code DLJ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANNABINOID URINE DRUGS OF ABUSE CALIBRATORS AND CONTROLS?

CANNABINOID URINE DRUGS OF ABUSE CALIBRATORS AND CONTROLS is a medical device that received FDA 510(k) clearance on 2002-06-18. The listed applicant is Lin-Zhi International, Inc.. The 510(k) number is K021449.

When did CANNABINOID URINE DRUGS OF ABUSE CALIBRATORS AND CONTROLS receive FDA 510(k) clearance?

CANNABINOID URINE DRUGS OF ABUSE CALIBRATORS AND CONTROLS received FDA 510(k) clearance on 2002-06-18, under 510(k) number K021449.

Who is the listed applicant for CANNABINOID URINE DRUGS OF ABUSE CALIBRATORS AND CONTROLS?

The FDA 510(k) record lists Lin-Zhi International, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CANNABINOID URINE DRUGS OF ABUSE CALIBRATORS AND CONTROLS?

The FDA product code for CANNABINOID URINE DRUGS OF ABUSE CALIBRATORS AND CONTROLS is DLJ.

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 Lin-Zhi International, 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.

View all 43 devices →

Related Devices (Code: DLJ)

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

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

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