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FDA 510(k)

ACA DU PONT URINE CANNABINOIDS (U THC) SCREEN METH

K-Number: K875252 · 1988-02-03

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1988-02-03
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ACA DU PONT URINE CANNABINOIDS (U THC) SCREEN METH 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 1988-02-03 under 510(k) number K875252. 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 ACA DU PONT URINE CANNABINOIDS (U THC) SCREEN METH?

ACA DU PONT URINE CANNABINOIDS (U THC) SCREEN METH is a medical device that received FDA 510(k) clearance on 1988-02-03. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K875252.

When did ACA DU PONT URINE CANNABINOIDS (U THC) SCREEN METH receive FDA 510(k) clearance?

ACA DU PONT URINE CANNABINOIDS (U THC) SCREEN METH received FDA 510(k) clearance on 1988-02-03, under 510(k) number K875252.

Who is the listed applicant for ACA DU PONT URINE CANNABINOIDS (U THC) SCREEN METH?

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 CANNABINOIDS (U THC) SCREEN METH?

The FDA product code for ACA DU PONT URINE CANNABINOIDS (U THC) SCREEN METH is LDJ.

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

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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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