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FDA 510(k)

QUIKSTRIP ONE STEP OPIATES TEST

K-Number: K972571 · 1997-08-20

ApplicantDrial Consultants, Inc.
Decision Date1997-08-20
Product CodeDJG
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

QUIKSTRIP ONE STEP OPIATES 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 1997-08-20 under 510(k) number K972571. The device is classified under product code DJG. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUIKSTRIP ONE STEP OPIATES TEST?

QUIKSTRIP ONE STEP OPIATES TEST is a medical device that received FDA 510(k) clearance on 1997-08-20. The listed applicant is Drial Consultants, Inc.. The 510(k) number is K972571.

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

QUIKSTRIP ONE STEP OPIATES TEST received FDA 510(k) clearance on 1997-08-20, under 510(k) number K972571.

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

The FDA product code for QUIKSTRIP ONE STEP OPIATES TEST is DJG.

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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.

K973269QUIKSTRIP ONE STEP BENZODIAZEPINE TESTK973326QUIKPAC II ONE STEP BENZODIAZEPINE TESTK973047ONE STEP URINE DRUG OF ABUSE BARBITURATE TESTK972059QUIKPAC II ONE STEP COCAINE TESTK972405QUIKPAC II ONE STEP OPIATE TESTK971926QUIKSTRIP ONE STEP COCAINE TEST

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Related Devices (Code: DJG)

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.

K252684Labcorp Fentanyl Urine Visual TestMedtox Diagnostics, Inc.K250741Evidence MultiSTAT DOA Urine MultiPlexRandox Laboratories LimitedK253082LZI Buprenorphine II Enzyme ImmunoassayLin-Zhi International, Inc.K252520SEFRIA™ Hydrocodone Oral FluidImmunalysis CorporationK251972Healgen® AccuFluor Fentanyl Fluorescence Immunoassay (FIA)Test Kit - Qualitative; Healgen® Immunofluorescence Analyzer (OG-H180)Healgen Scientific,, LLCK251634LZI Fentanyl III Enzyme ImmunoassayLin-Zhi International, Inc.

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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