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FDA 510(k)

QUIKSTRIP ONE STEP BENZODIAZEPINE TEST

K-Number: K973269 · 1998-02-25

Decision Date1998-02-25
Product CodeJXM
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

QUIKSTRIP ONE STEP BENZODIAZEPINE TEST is the device name listed in this FDA 510(k) record. The listed applicant is Drial Consultants, Inc.. It received FDA 510(k) clearance on 1998-02-25 under 510(k) number K973269. 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 QUIKSTRIP ONE STEP BENZODIAZEPINE TEST?

QUIKSTRIP ONE STEP BENZODIAZEPINE TEST is a medical device that received FDA 510(k) clearance on 1998-02-25. The listed applicant is Drial Consultants, Inc.. The 510(k) number is K973269.

When did QUIKSTRIP ONE STEP BENZODIAZEPINE TEST receive FDA 510(k) clearance?

QUIKSTRIP ONE STEP BENZODIAZEPINE TEST received FDA 510(k) clearance on 1998-02-25, under 510(k) number K973269.

Who is the listed applicant for QUIKSTRIP ONE STEP BENZODIAZEPINE TEST?

The FDA 510(k) record lists Drial Consultants, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUIKSTRIP ONE STEP BENZODIAZEPINE TEST?

The FDA product code for QUIKSTRIP ONE STEP BENZODIAZEPINE TEST is JXM.

Related Clinical Trials

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.

Other records listing Drial Consultants, 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.

View all 13 devices →

Related Devices (Code: JXM)

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.

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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