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FDA 510(k)

EMIT 700 COCAINE METABOLITE ASSAY

K-Number: K843160 · 1984-08-29

ApplicantSyva Co.
Decision Date1984-08-29
Product CodeDIO
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

EMIT 700 COCAINE METABOLITE ASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Syva Co.. It received FDA 510(k) clearance on 1984-08-29 under 510(k) number K843160. 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 EMIT 700 COCAINE METABOLITE ASSAY?

EMIT 700 COCAINE METABOLITE ASSAY is a medical device that received FDA 510(k) clearance on 1984-08-29. The listed applicant is Syva Co.. The 510(k) number is K843160.

When did EMIT 700 COCAINE METABOLITE ASSAY receive FDA 510(k) clearance?

EMIT 700 COCAINE METABOLITE ASSAY received FDA 510(k) clearance on 1984-08-29, under 510(k) number K843160.

Who is the listed applicant for EMIT 700 COCAINE METABOLITE ASSAY?

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

What is the FDA product code for EMIT 700 COCAINE METABOLITE ASSAY?

The FDA product code for EMIT 700 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 Syva Co. 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 448 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

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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