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FDA 510(k)

AUTOMATES COMA COCAINE METABOLITE ASSAY

K-Number: K921834 · 1992-06-15

ApplicantSerex, Inc.
Decision Date1992-06-15
Product CodeDIO
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

AUTOMATES COMA COCAINE METABOLITE ASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Serex, Inc.. It received FDA 510(k) clearance on 1992-06-15 under 510(k) number K921834. The device is classified under product code DIO. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATES COMA COCAINE METABOLITE ASSAY?

AUTOMATES COMA COCAINE METABOLITE ASSAY is a medical device that received FDA 510(k) clearance on 1992-06-15. The listed applicant is Serex, Inc.. The 510(k) number is K921834.

When did AUTOMATES COMA COCAINE METABOLITE ASSAY receive FDA 510(k) clearance?

AUTOMATES COMA COCAINE METABOLITE ASSAY received FDA 510(k) clearance on 1992-06-15, under 510(k) number K921834.

Who is the listed applicant for AUTOMATES COMA COCAINE METABOLITE ASSAY?

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

What is the FDA product code for AUTOMATES COMA COCAINE METABOLITE ASSAY?

The FDA product code for AUTOMATES COMA COCAINE METABOLITE ASSAY is DIO.

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 Serex, 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.

Related Devices (Code: DIO)

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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