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

Sysmex UD-10, Fully Automated Urine Particle Digital Imaging Device

K Number: K182062 · Decision Oct 30, 2018
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
34
Applicant Total
31
Review Days
90

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Basic Information

Device Name
Sysmex UD-10, Fully Automated Urine Particle Digital Imaging Device
K Number
K182062
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5260
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sysmex America, Inc.
Date Received
August 1, 2018
Decision Date
October 30, 2018
Product Code
JOY
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
JOY Device, Automated Cell-Locating

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JOY), ordered by most recent decision date.

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Other Clearances by Sysmex America, Inc.

K Number Device Name
K253212 XR-Series (XR-10, XR-20) Automated Hematology Analyzers
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
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. →