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FDA 510(k)

DRUG OF ABUSE ANALYSIS SYSTEM

K-Number: K903825 · 1990-09-27

Decision Date1990-09-27
Product CodeDIS
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

DRUG OF ABUSE ANALYSIS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Technicon Instruments Corp.. It received FDA 510(k) clearance on 1990-09-27 under 510(k) number K903825. The device is classified under product code DIS. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRUG OF ABUSE ANALYSIS SYSTEM?

DRUG OF ABUSE ANALYSIS SYSTEM is a medical device that received FDA 510(k) clearance on 1990-09-27. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K903825.

When did DRUG OF ABUSE ANALYSIS SYSTEM receive FDA 510(k) clearance?

DRUG OF ABUSE ANALYSIS SYSTEM received FDA 510(k) clearance on 1990-09-27, under 510(k) number K903825.

Who is the listed applicant for DRUG OF ABUSE ANALYSIS SYSTEM?

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

What is the FDA product code for DRUG OF ABUSE ANALYSIS SYSTEM?

The FDA product code for DRUG OF ABUSE ANALYSIS SYSTEM is DIS.

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 Technicon Instruments Corp. 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.

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Related Devices (Code: DIS)

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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