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

SKR 3000

K Number: K223267 · Decision Nov 17, 2022
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
422
Applicant Total
25
Review Days
24

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Basic Information

Device Name
SKR 3000
K Number
K223267
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Konica Minolta, Inc.
Date Received
October 24, 2022
Decision Date
November 17, 2022
Product Code
MQB
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
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

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Other Clearances by Konica Minolta, Inc.

K Number Device Name
K250665 SKR 3000
K241319 SKR 3000
K240281 Bone Suppression Software
K230906 Konicaminolta DI-X1
K220993 Ultrasound System SONIMAGE MX1
K213908 SKR 3000
K212685 KONICAMINOLTA DI-X1
K210619 SKR 3000
K210066 ImagePilot
K191645 SKR 4000
Search all 25 clearances from Konica Minolta, Inc. →