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FDA 510(k)

MICRO EIA FOR COCAINE METABOLITES

K-Number: K914533 · 1991-12-10

Decision Date1991-12-10
Product CodeDIO
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

MICRO EIA FOR COCAINE METABOLITES is the device name listed in this FDA 510(k) record. The listed applicant is Microdiagnostics, Inc.. It received FDA 510(k) clearance on 1991-12-10 under 510(k) number K914533. 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 MICRO EIA FOR COCAINE METABOLITES?

MICRO EIA FOR COCAINE METABOLITES is a medical device that received FDA 510(k) clearance on 1991-12-10. The listed applicant is Microdiagnostics, Inc.. The 510(k) number is K914533.

When did MICRO EIA FOR COCAINE METABOLITES receive FDA 510(k) clearance?

MICRO EIA FOR COCAINE METABOLITES received FDA 510(k) clearance on 1991-12-10, under 510(k) number K914533.

Who is the listed applicant for MICRO EIA FOR COCAINE METABOLITES?

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

What is the FDA product code for MICRO EIA FOR COCAINE METABOLITES?

The FDA product code for MICRO EIA FOR COCAINE METABOLITES 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 Microdiagnostics, 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 10 devices →

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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