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FDA 510(k)

DRUGS OF ABUSE CONTROLS

K-Number: K935285 · 1994-03-22

ApplicantMedical Diagnostic Technologies, Inc.
Decision Date1994-03-22
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

DRUGS OF ABUSE CONTROLS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Diagnostic Technologies, Inc.. It received FDA 510(k) clearance on 1994-03-22 under 510(k) number K935285. 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 DRUGS OF ABUSE CONTROLS?

DRUGS OF ABUSE CONTROLS is a medical device that received FDA 510(k) clearance on 1994-03-22. The listed applicant is Medical Diagnostic Technologies, Inc.. The 510(k) number is K935285.

When did DRUGS OF ABUSE CONTROLS receive FDA 510(k) clearance?

DRUGS OF ABUSE CONTROLS received FDA 510(k) clearance on 1994-03-22, under 510(k) number K935285.

Who is the listed applicant for DRUGS OF ABUSE CONTROLS?

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

What is the FDA product code for DRUGS OF ABUSE CONTROLS?

The FDA product code for DRUGS OF ABUSE CONTROLS is DIF.

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Other records listing Medical Diagnostic Technologies, Inc. as applicant

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Related Devices (Code: DIF)

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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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