510(k) K251371

Sysmex XR-Series (XR-20) Automated Hematology Analyzer by Sysmex America, Inc. — Product Code GKZ

K251371 is an FDA 510(k) premarket notification submitted by Sysmex America, Inc. for the device "Sysmex XR-Series (XR-20) Automated Hematology Analyzer". The FDA issued a decision of Substantially Equivalent on June 25, 2025. The device falls under product code GKZ (Counter, Differential Cell), a Class II device regulated under 21 CFR 864.5220. Sysmex America, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 25, 2025
Date Received
May 2, 2025
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Counter, Differential Cell
Device Class
Class II
Regulation Number
864.5220
Review Panel
HE
Submission Type