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FDA 510(k)

QUANTIMETRIX URINE DRUGS OF ABUSE CONTROL

K-Number: K873467 · 1987-09-29

ApplicantQuantimetrix Medical Industries
Decision Date1987-09-29
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

QUANTIMETRIX URINE DRUGS OF ABUSE CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Quantimetrix Medical Industries. It received FDA 510(k) clearance on 1987-09-29 under 510(k) number K873467. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTIMETRIX URINE DRUGS OF ABUSE CONTROL?

QUANTIMETRIX URINE DRUGS OF ABUSE CONTROL is a medical device that received FDA 510(k) clearance on 1987-09-29. The listed applicant is Quantimetrix Medical Industries. The 510(k) number is K873467.

When did QUANTIMETRIX URINE DRUGS OF ABUSE CONTROL receive FDA 510(k) clearance?

QUANTIMETRIX URINE DRUGS OF ABUSE CONTROL received FDA 510(k) clearance on 1987-09-29, under 510(k) number K873467.

Who is the listed applicant for QUANTIMETRIX URINE DRUGS OF ABUSE CONTROL?

The FDA 510(k) record lists Quantimetrix Medical Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUANTIMETRIX URINE DRUGS OF ABUSE CONTROL?

The FDA product code for QUANTIMETRIX URINE DRUGS OF ABUSE CONTROL is DIF.

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Other records listing Quantimetrix Medical Industries 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.

K895778QUANTIMETRIX BILIRUBIN CALIBRATORSK883395ALKPHOR(TM) SYSTEM, HUMAN SERUM ALKA PHOS ISOENZYK883247LIPOPHOR(TM) SYST, HUMAN SERUM LIPOPROTEIN CONTROLK874302QUANTIMETRIX TOTAL CREATINE KINASE CONTROLK874890QUANTIMETRIX URINE DIPSTICK CONTROLK873011QUANTIMETRIX SERUM ALCOHOL CONTROL LEVEL 1 AND 2

View all 8 devices →

Related Devices (Code: DIF)

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.

K153474Detectabuse Liquid Control Urine, Detectabuse Stat-Skreen Liquid Control Urine, Detectabuse Liquid Control Urine, AU/NZ, Detectabuse Liquid Control Urine, Immunoassay Series, Detectabuse Liquid Control Urine, GC/MS and Confirm seriesBiochemical Diagnostics, Inc.K132688SALIVABUSE LIQUID ORAL FLUID CONTROL, SALIVABUSE LIQUID ORAL FLUID CONTROL, AU/NZBiochemical Diagnostics, Inc.K132174MULTICHEM WBTTechno-Path Manufacturing , Ltd.K121122DETECTABUSE LIQUID CONTROL, DETECTABUSE STAT-SKREEN LIQUID CONTROLBiochemical Diagnostic, Inc.K121143LIQUICHEK WHOLE BLOOD IMMUNOSUPPRESSANT CONTROL TILEVEL (1,2 AND 3)Bio-Rad LaboratoriesK120504LIQUICHEK URINE TOXICOLOGY CONTROL, S10 & S10 MINIPAK, LIQUICHEK URINE TOXICOLOGY CONTROL, LEVEL S20 & LEVEL S20 MINIPAKBio-Rad Laboratories, 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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