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FDA 510(k)

URINE BENZODIAZEPINES SCREEN FLEX TEAGENT CARTRIDGE

K-Number: K950427 · 1995-03-21

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1995-03-21
Product CodeJXM
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

URINE BENZODIAZEPINES SCREEN FLEX TEAGENT CARTRIDGE 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 1995-03-21 under 510(k) number K950427. 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 URINE BENZODIAZEPINES SCREEN FLEX TEAGENT CARTRIDGE?

URINE BENZODIAZEPINES SCREEN FLEX TEAGENT CARTRIDGE is a medical device that received FDA 510(k) clearance on 1995-03-21. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K950427.

When did URINE BENZODIAZEPINES SCREEN FLEX TEAGENT CARTRIDGE receive FDA 510(k) clearance?

URINE BENZODIAZEPINES SCREEN FLEX TEAGENT CARTRIDGE received FDA 510(k) clearance on 1995-03-21, under 510(k) number K950427.

Who is the listed applicant for URINE BENZODIAZEPINES SCREEN FLEX TEAGENT CARTRIDGE?

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 URINE BENZODIAZEPINES SCREEN FLEX TEAGENT CARTRIDGE?

The FDA product code for URINE BENZODIAZEPINES SCREEN FLEX TEAGENT CARTRIDGE is JXM.

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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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