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FDA 510(k)

Sysmex XQ-Series (XQ-320) Automated Hematology Analyzer

K-Number: K230887 · 2023-12-21

Decision Date2023-12-21
Product CodeGKZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

Sysmex XQ-Series (XQ-320) Automated Hematology Analyzer is a medical device manufactured by Sysmex America, Inc.. It received FDA 510(k) clearance on 2023-12-21 under approval number K230887. The device is classified under product code GKZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sysmex XQ-Series (XQ-320) Automated Hematology Analyzer?

Sysmex XQ-Series (XQ-320) Automated Hematology Analyzer is a medical device that received FDA 510(k) clearance on 2023-12-21. It is manufactured by Sysmex America, Inc.. The 510(k) number is K230887.

When was Sysmex XQ-Series (XQ-320) Automated Hematology Analyzer approved by the FDA?

Sysmex XQ-Series (XQ-320) Automated Hematology Analyzer received FDA 510(k) clearance on 2023-12-21, under approval number K230887.

What company makes Sysmex XQ-Series (XQ-320) Automated Hematology Analyzer?

Sysmex XQ-Series (XQ-320) Automated Hematology Analyzer is manufactured by Sysmex America, Inc..

What is the FDA product code for Sysmex XQ-Series (XQ-320) Automated Hematology Analyzer?

The FDA product code for Sysmex XQ-Series (XQ-320) Automated Hematology Analyzer is GKZ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.