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FDA 510(k)

EMIT 700 CANNABINOID ASSAY

K-Number: K843421 · 1984-09-25

ApplicantSyva Co.
Decision Date1984-09-25
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

EMIT 700 CANNABINOID 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 1984-09-25 under 510(k) number K843421. 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 ASSAY?

EMIT 700 CANNABINOID ASSAY is a medical device that received FDA 510(k) clearance on 1984-09-25. The listed applicant is Syva Co.. The 510(k) number is K843421.

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

EMIT 700 CANNABINOID ASSAY received FDA 510(k) clearance on 1984-09-25, under 510(k) number K843421.

Who is the listed applicant for EMIT 700 CANNABINOID 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 ASSAY?

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

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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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