Canon Medical Systems Corporation

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
95
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K260078Aquilion ServeSP (TSX-307B) V2.0March 13, 2026
K253584Alphenix, INFX-8000V/B, INFX-8000V/S, V9.6 with aEvolve Imaging (FOV Extension)March 10, 2026
K253597Aplio beyond and Aplio me Software V2.0 Diagnostic Ultrasound SystemJanuary 20, 2026
K251370Cartesion Prime (PCD-1000A/3) V10.21December 1, 2025
K252074Aplio i900, Aplio i800 and Aplio i700 Software V9.0 Diagnostic Ultrasound SystemOctober 31, 2025
K251602Alphenix, INFX-8000V/B, INFX-8000V/S, V9.6 with aEvolve ImagingOctober 10, 2025
K251645Self-Propelled CT Scan Base Kit, CGBA-035A; Alphenix, INFX-8000C/B, INFX-8000C/S, V9.6 with CalculatSeptember 26, 2025
K250901Vantage Fortian/Orian 1.5T, MRT-1550, V10.0 with AiCE Reconstruction Processing Unit for MRJuly 22, 2025
K243398CT Scanner TSX-501R/1 V11.1June 20, 2025
K242808Aplio i900/i800/i700 Diagnostic Ultrasound System, Software V8.5May 13, 2025
K250328UltraExtend NX CUW-U001S V2.0 Ultrasound Image Analysis ProgramApril 30, 2025
K243335Vantage Galan 3T, MRT-3020, V10.0 with AiCE Reconstruction Processing Unit for MRJanuary 7, 2025
K242403Aquilion ONE (TSX-308A/3) V1.5December 23, 2024
K241582Aplio i900/i800/i700 Diagnostic Ultrasound System, Software V7.0 (TUS-AI900, TUS-AI800, TUS-AI700)September 12, 2024
K233107Alphenix, INFX-8000V/B, INFX-8000V/S, V9.5August 30, 2024
K241496Vantage Galan 3T, MRT-3020, V10.0 with AiCE Reconstruction Processing Unit for MRAugust 20, 2024
K240705Vitrea Software Package, VSTP-002A V2.0July 17, 2024
K240238Vantage Fortian/Orian 1.5T, MRT-1550, V9.0 with AiCE Reconstruction Processing Unit for MRApril 12, 2024
K232835Aquilion ONE (TSX-308A/3) V1.4 with PIQE Reconstruction SystemApril 2, 2024
K233195Aplio i900, Aplio i800 and Aplio i700 Software V8.1 Diagnostic Ultrasound SystemJanuary 24, 2024