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FDA 510(k)

ROCHE ABUSCREEN TRI-LEVEL REFERENCE CONTROLS

K-Number: K932753 · 1993-07-22

ApplicantRoche Diagnostic Systems, Inc.
Decision Date1993-07-22
Product CodeDKB
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ROCHE ABUSCREEN TRI-LEVEL REFERENCE CONTROLS 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 1993-07-22 under 510(k) number K932753. The device is classified under product code DKB. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROCHE ABUSCREEN TRI-LEVEL REFERENCE CONTROLS?

ROCHE ABUSCREEN TRI-LEVEL REFERENCE CONTROLS is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Roche Diagnostic Systems, Inc.. The 510(k) number is K932753.

When did ROCHE ABUSCREEN TRI-LEVEL REFERENCE CONTROLS receive FDA 510(k) clearance?

ROCHE ABUSCREEN TRI-LEVEL REFERENCE CONTROLS received FDA 510(k) clearance on 1993-07-22, under 510(k) number K932753.

Who is the listed applicant for ROCHE ABUSCREEN TRI-LEVEL REFERENCE CONTROLS?

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 TRI-LEVEL REFERENCE CONTROLS?

The FDA product code for ROCHE ABUSCREEN TRI-LEVEL REFERENCE CONTROLS is DKB.

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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: DKB)

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.

K120936ABBOTT TDM MULTICONSTITUENT CALIBRATOR, THERMO SCIENTIFIC QMS MULTI-CONSTITUENT CALIBRATORSMicrogenics CorporationK092266RANDOX METHAMPHETAMINE ASSAYRandox Laboratories, Ltd.K101752THERMO SCIENTIFIC CEDIA MULTI-DRUG OFT CALIBRATORSMicrogenics Corp.K090939ROCHE C.F.A.S. DAT QUALITATIVE PLUS CLINICAL CALIBRATOR AND CONTROL SET DAT CLINICAL, MODELS 04590856 190, 04500873 190Roche DiagnosticsK090900ADVIA CHEMISTRY DRUG CALIBRATOR II, MODEL 10376771Siemens Healthcare DiagnosticsK062162DIMENSION VISTA SYSTEM DRUGS OF ABUSE CALIBRATOR (UDAT CAL - KC510)Dade Behring, 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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