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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 a medical device manufactured by Siemens Healthcare Diagnostics, Inc.. It received FDA 510(k) clearance on 2020-02-13 under approval 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. It is manufactured by Siemens Healthcare Diagnostics, Inc.. The 510(k) number is K193489.

When was ADVIA Centaur BR approved by the FDA?

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

What company makes ADVIA Centaur BR?

ADVIA Centaur BR is manufactured by Siemens Healthcare Diagnostics, Inc..

What is the FDA product code for ADVIA Centaur BR?

The FDA product code for ADVIA Centaur BR is MOI.

Other Devices by Siemens Healthcare Diagnostics, Inc.

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Related Devices (Code: MOI)

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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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