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FDA 510(k)

COBAS-FP TDM CONTROLS

K-Number: K930269 · 1993-02-25

ApplicantRoche Diagnostic Systems, Inc.
Decision Date1993-02-25
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

COBAS-FP TDM 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 1993-02-25 under 510(k) number K930269. 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 COBAS-FP TDM CONTROLS?

COBAS-FP TDM CONTROLS is a medical device that received FDA 510(k) clearance on 1993-02-25. The listed applicant is Roche Diagnostic Systems, Inc.. The 510(k) number is K930269.

When did COBAS-FP TDM CONTROLS receive FDA 510(k) clearance?

COBAS-FP TDM CONTROLS received FDA 510(k) clearance on 1993-02-25, under 510(k) number K930269.

Who is the listed applicant for COBAS-FP TDM 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 COBAS-FP TDM CONTROLS?

The FDA product code for COBAS-FP TDM CONTROLS is DIF.

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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

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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