Sysmex XQ-Series (XQ-320) Automated Hematology Analyzer
K-Number: K230887 · 2023-12-21
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.