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FDA 510(k)

ACA DU PONT URINE COCAINE METABOLITE (U COC)SCREEN

K-Number: K874213 · 1987-11-13

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1987-11-13
Product CodeDIO
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ACA DU PONT URINE COCAINE METABOLITE (U COC)SCREEN is the device name listed in this FDA 510(k) record. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. It received FDA 510(k) clearance on 1987-11-13 under 510(k) number K874213. 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 ACA DU PONT URINE COCAINE METABOLITE (U COC)SCREEN?

ACA DU PONT URINE COCAINE METABOLITE (U COC)SCREEN is a medical device that received FDA 510(k) clearance on 1987-11-13. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K874213.

When did ACA DU PONT URINE COCAINE METABOLITE (U COC)SCREEN receive FDA 510(k) clearance?

ACA DU PONT URINE COCAINE METABOLITE (U COC)SCREEN received FDA 510(k) clearance on 1987-11-13, under 510(k) number K874213.

Who is the listed applicant for ACA DU PONT URINE COCAINE METABOLITE (U COC)SCREEN?

The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACA DU PONT URINE COCAINE METABOLITE (U COC)SCREEN?

The FDA product code for ACA DU PONT URINE COCAINE METABOLITE (U COC)SCREEN is DIO.

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Other records listing E.I. Dupont DE Nemours & Co., Inc. as applicant

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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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