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. The listed applicant is Sysmex America, Inc.. The 510(k) number is K230887.
When did Sysmex XQ-Series (XQ-320) Automated Hematology Analyzer receive FDA 510(k) clearance?
Sysmex XQ-Series (XQ-320) Automated Hematology Analyzer received FDA 510(k) clearance on 2023-12-21, under 510(k) number K230887.
Who is the listed applicant for Sysmex XQ-Series (XQ-320) Automated Hematology Analyzer?
The FDA 510(k) record lists Sysmex America, Inc. as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Sysmex America, Inc. as applicant
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.
Related Devices (Code: GKZ)
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.
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.