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FDA 510(k)

ADVIA Centaur BR

K-Number: K193489 · 2020-02-13

ApplicantSiemens Healthcare Diagnostics, Inc.
Decision Date2020-02-13
Product CodeMOI
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

ADVIA Centaur BR is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Healthcare Diagnostics, Inc.. It received FDA 510(k) clearance on 2020-02-13 under 510(k) number K193489. The device is classified under product code MOI. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVIA Centaur BR?

ADVIA Centaur BR is a medical device that received FDA 510(k) clearance on 2020-02-13. The listed applicant is Siemens Healthcare Diagnostics, Inc.. The 510(k) number is K193489.

When did ADVIA Centaur BR receive FDA 510(k) clearance?

ADVIA Centaur BR received FDA 510(k) clearance on 2020-02-13, under 510(k) number K193489.

Who is the listed applicant for ADVIA Centaur BR?

The FDA 510(k) record lists Siemens Healthcare Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ADVIA Centaur BR?

The FDA product code for ADVIA Centaur BR is MOI.

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Related Devices (Code: MOI)

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K240403Access BR MonitorBeckman Coulter, Inc.K233946IMMULITE® 2000 BR-MASiemens Healthcare Diagnostics Products, Ltd.K192524Lumipulse G CA15-3Fujirebio Diagnostics,Inc.K192777ADVIA Centaur CA 15-3 assaySiemens Healthcare Diagnostics, Inc.K181492Elecsys CA 15-3 IIRoche DiagnosticsK171605Elecsys CA 15-3 IIRoche Diagnostics

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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