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

CT Scanner TSX-501R/1 V11.1

K Number: K243398 · Decision Jun 20, 2025
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
795
Applicant Total
87
Review Days
232

Basic Information

Device Name
CT Scanner TSX-501R/1 V11.1
K Number
K243398
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Canon Medical Systems Corporation
Date Received
October 31, 2024
Decision Date
June 20, 2025
Product Code
JAK
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
JAK System, X-Ray, Tomography, Computed

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