FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

XR-Series (XR-10, XR-20) Automated Hematology Analyzers

K Number: K253212 · Decision May 27, 2026
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
379
Applicant Total
31
Review Days
240

Basic Information

Device Name
XR-Series (XR-10, XR-20) Automated Hematology Analyzers
K Number
K253212
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5220
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sysmex America, Inc.
Date Received
September 29, 2025
Decision Date
May 27, 2026
Product Code
GKZ
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GKZ Counter, Differential Cell

Similar 510(k) Clearances

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Other Clearances by Sysmex America, Inc.

K Number Device Name
K250943 Sysmex XR-Series (XR-10) Automated Hematology Analyzer
K251371 Sysmex XR-Series (XR-20) Automated Hematology Analyzer
K250965 Automated Blood Coagulation Analyzer CN-Series (CN-6000)
K230887 Sysmex XQ-Series (XQ-320) Automated Hematology Analyzer
K210346 Sysmex XW-100 Automated Hematology Analyzer
K182389 Sysmex XN-L Automated Hematology Analyzer
K182062 Sysmex UD-10, Fully Automated Urine Particle Digital Imaging Device
K171883 Sysmex UF-5000 Fully Automated Urine Particle Analyzer
K172604 XW-100 Automated Hematology Analyzer for CLIA Waived Use
K160538 Sysmex XN-L Automated Hematology Analyzer
Search all 31 clearances from Sysmex America, Inc. →