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FDA 510(k)

EMIT 700 CANNABINOID 20 ASSAY

K-Number: K851373 · 1985-05-01

ApplicantSyva Co.
Decision Date1985-05-01
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

EMIT 700 CANNABINOID 20 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 1985-05-01 under 510(k) number K851373. The device is classified under product code LDJ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMIT 700 CANNABINOID 20 ASSAY?

EMIT 700 CANNABINOID 20 ASSAY is a medical device that received FDA 510(k) clearance on 1985-05-01. The listed applicant is Syva Co.. The 510(k) number is K851373.

When did EMIT 700 CANNABINOID 20 ASSAY receive FDA 510(k) clearance?

EMIT 700 CANNABINOID 20 ASSAY received FDA 510(k) clearance on 1985-05-01, under 510(k) number K851373.

Who is the listed applicant for EMIT 700 CANNABINOID 20 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 CANNABINOID 20 ASSAY?

The FDA product code for EMIT 700 CANNABINOID 20 ASSAY is LDJ.

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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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