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FDA 510(k)

ACA URINE BENZODIAZEPINES (UBENZ) SCREEN METHOD

K-Number: K873538 · 1987-10-02

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1987-10-02
Product CodeJXM
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ACA URINE BENZODIAZEPINES (UBENZ) SCREEN METHOD 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 1987-10-02 under 510(k) number K873538. The device is classified under product code JXM. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACA URINE BENZODIAZEPINES (UBENZ) SCREEN METHOD?

ACA URINE BENZODIAZEPINES (UBENZ) SCREEN METHOD is a medical device that received FDA 510(k) clearance on 1987-10-02. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K873538.

When did ACA URINE BENZODIAZEPINES (UBENZ) SCREEN METHOD receive FDA 510(k) clearance?

ACA URINE BENZODIAZEPINES (UBENZ) SCREEN METHOD received FDA 510(k) clearance on 1987-10-02, under 510(k) number K873538.

Who is the listed applicant for ACA URINE BENZODIAZEPINES (UBENZ) SCREEN METHOD?

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 URINE BENZODIAZEPINES (UBENZ) SCREEN METHOD?

The FDA product code for ACA URINE BENZODIAZEPINES (UBENZ) SCREEN METHOD is JXM.

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

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Related Devices (Code: JXM)

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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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