FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

RadiForce GX570; RadiForce GX570-AR

K Number: K252030 · Decision Aug 28, 2025
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
134
Applicant Total
29
Review Days
59

Basic Information

Device Name
RadiForce GX570; RadiForce GX570-AR
K Number
K252030
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Eizo Corporation
Date Received
June 30, 2025
Decision Date
August 28, 2025
Product Code
PGY
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
PGY Display, Diagnostic Radiology

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Other Clearances by Eizo Corporation

K Number Device Name
K242545 RadiForce MX317W-PA
K243221 RadiForce RX570; RadiForce RX570-AR
K241441 RadiForce RX670; RadiForce RX670-AR
K233465 RadiForce MX317W
K231066 CuratOR EX3242-FD
K230684 RadiForce MX217
K223768 RadiForce RX270
K221136 RadiForce MX243W
K211491 RadiForce RX370
K200485 RadiForce RX1270, RadiForce RX1270-AR
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