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FDA 510(k)

ROCHE ABUSCREEN ONTRAK POS. REF. CONTROL-METHADONE

K-Number: K930844 · 1994-01-27

ApplicantRoche Diagnostic Systems, Inc.
Decision Date1994-01-27
Product CodeLAS
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ROCHE ABUSCREEN ONTRAK POS. REF. CONTROL-METHADONE 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 1994-01-27 under 510(k) number K930844. The device is classified under product code LAS. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROCHE ABUSCREEN ONTRAK POS. REF. CONTROL-METHADONE?

ROCHE ABUSCREEN ONTRAK POS. REF. CONTROL-METHADONE is a medical device that received FDA 510(k) clearance on 1994-01-27. The listed applicant is Roche Diagnostic Systems, Inc.. The 510(k) number is K930844.

When did ROCHE ABUSCREEN ONTRAK POS. REF. CONTROL-METHADONE receive FDA 510(k) clearance?

ROCHE ABUSCREEN ONTRAK POS. REF. CONTROL-METHADONE received FDA 510(k) clearance on 1994-01-27, under 510(k) number K930844.

Who is the listed applicant for ROCHE ABUSCREEN ONTRAK POS. REF. CONTROL-METHADONE?

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 ROCHE ABUSCREEN ONTRAK POS. REF. CONTROL-METHADONE?

The FDA product code for ROCHE ABUSCREEN ONTRAK POS. REF. CONTROL-METHADONE is LAS.

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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: LAS)

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.

K080459CHROMESYTEMS TOXICOLOGY CALIBRATORS AND CONTROLSChromsystems Instruments & Chemicals GmbHK072257MYCOPHENOLIC ACID CONTROL, LEVEL 1, 2, 3, 4, 4-LEVELMore DiagnosticsK062942QUANTIMETRIX NICOSURE COTININE URINE CONTROLQuantimetrix Corp.K051074MAS IMMUNOSUPPRESSANT CONTROLSMicrogenics Corp.K040411DRI OXYCODONE ASSAYMicrogenics Corp.K032842MICROGENICS CYCLOSPORINE CONTROL KITMicrogenics Corp.

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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