510(k) K250665

Device
SKR 3000
Applicant
Konica Minolta, Inc.
510(k) number
K250665
Product code
MQB
Decision
Substantially Equivalent (SESE)
Decision date
2025-06-17
Date received
2025-03-05
Regulation
892.1680
Classification name
Solid State X-Ray Imager (Flat Panel/Digital Imager)
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Makoto Sumi
Address
1 Sakura-Machi Hino-Shi Tokyo JP 1918511 1918511

FDA Registration Numbers

Source Documents

510(k) summary PDF

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