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FDA 510(k)

EMIT D.A.U. CANNABINOID 50 NG ASSAY & CALIBRATORS

K-Number: K882313 · 1988-08-29

ApplicantSyva Co.
Decision Date1988-08-29
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

EMIT D.A.U. CANNABINOID 50 NG ASSAY & CALIBRATORS is the device name listed in this FDA 510(k) record. The listed applicant is Syva Co.. It received FDA 510(k) clearance on 1988-08-29 under 510(k) number K882313. 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 D.A.U. CANNABINOID 50 NG ASSAY & CALIBRATORS?

EMIT D.A.U. CANNABINOID 50 NG ASSAY & CALIBRATORS is a medical device that received FDA 510(k) clearance on 1988-08-29. The listed applicant is Syva Co.. The 510(k) number is K882313.

When did EMIT D.A.U. CANNABINOID 50 NG ASSAY & CALIBRATORS receive FDA 510(k) clearance?

EMIT D.A.U. CANNABINOID 50 NG ASSAY & CALIBRATORS received FDA 510(k) clearance on 1988-08-29, under 510(k) number K882313.

Who is the listed applicant for EMIT D.A.U. CANNABINOID 50 NG ASSAY & CALIBRATORS?

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 D.A.U. CANNABINOID 50 NG ASSAY & CALIBRATORS?

The FDA product code for EMIT D.A.U. CANNABINOID 50 NG ASSAY & CALIBRATORS 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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