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FDA 510(k)

ABUSCREEN(R) ONTRAK(R) POSITIVE REFERENCE CONTROL

K-Number: K914806 · 1991-11-19

ApplicantRoche Diagnostic Systems, Inc.
Decision Date1991-11-19
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ABUSCREEN(R) ONTRAK(R) POSITIVE REFERENCE CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Roche Diagnostic Systems, Inc.. It received FDA 510(k) clearance on 1991-11-19 under 510(k) number K914806. 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 ABUSCREEN(R) ONTRAK(R) POSITIVE REFERENCE CONTROL?

ABUSCREEN(R) ONTRAK(R) POSITIVE REFERENCE CONTROL is a medical device that received FDA 510(k) clearance on 1991-11-19. The listed applicant is Roche Diagnostic Systems, Inc.. The 510(k) number is K914806.

When did ABUSCREEN(R) ONTRAK(R) POSITIVE REFERENCE CONTROL receive FDA 510(k) clearance?

ABUSCREEN(R) ONTRAK(R) POSITIVE REFERENCE CONTROL received FDA 510(k) clearance on 1991-11-19, under 510(k) number K914806.

Who is the listed applicant for ABUSCREEN(R) ONTRAK(R) POSITIVE REFERENCE CONTROL?

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

What is the FDA product code for ABUSCREEN(R) ONTRAK(R) POSITIVE REFERENCE CONTROL?

The FDA product code for ABUSCREEN(R) ONTRAK(R) POSITIVE REFERENCE CONTROL is DIF.

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Other records listing Roche Diagnostic Systems, 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.

K983698MODIFICATION TO ABUSCREEN ONLINE BARBITURATESK983702MODIFICATION TO ABUSCREEN ONLINE FOR BENZOIDIAZEPINESK983704MODIFICATION TO ABUSCREEN ONLINE FOR PHENCYCLIDINEK983556ABUSCREEN ONLINE BENZ 300 CALIBRATORSK983555ABUSCREEN ONLINE BENZ 200 CALIBRATORSK983700MODIFICATION TO ABUSCREEN ONLINE FOR PROPOXYPHENE

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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