Toshibamedical Systems Corporation

FDA Regulatory Profile

Toshibamedical Systems Corporation has 0 FDA recalls, 0 inspections, 80 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Apr 20, 2018

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances80Oct 4, 2026Not statedCurrent
Inspections0Oct 23, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K173962Viamo c100 TUS-VC100 Diagnostic Ultrasound SystemApr 20, 2018
K173468Aquilion Precision (TSX-304A/2) V8.6 with FIRST 3.0Feb 23, 2018
K173088Vitrea Software Toshiba Package VSTP-001AJan 31, 2018
K173382Vantage Galan 3T, V4.6Jan 26, 2018
K173090Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V2.4Jan 11, 2018
K172863Infinix-i, INFX-8000V, V7.0Dec 14, 2017
K172276Xario 200 Diagnostic Ultrasound System V6.0Dec 12, 2017
K172646XIDF-AWS801, Angio Workstation, V7.0Oct 30, 2017
K171597Vantage Elan 1.5T, V4.0Jul 21, 2017
K170832Ultimax-i, DREX-UI80 V1.60Jul 21, 2017
K170177Aquilion ONE (TSX-305A/3) V8.3 with FIRST 2.1Jun 30, 2017
K171222Vitrea Software Toshiba Package; VSTP-001AJun 8, 2017
K170412Vantage Titan 1.5T, MRT-1510, M-Power GXJun 7, 2017
K170490Celesteion, PCA-9000A/3Jun 1, 2017
K163702Aplio i900/i800/i700 Diagnostic Ultrasound System, V2.1May 30, 2017
K170019Aquilion Lightning, TSX-036A/1, V8.4Feb 2, 2017
K162183Vantage Galan 3T, MRT-3020, V4.0Nov 25, 2016
K162155Xario 200 Diagnostic Ultrasound System V5.0Nov 1, 2016
K162614Infinix, INFX-8000V, V6.35Oct 17, 2016
K162187Xario 100 Diagnostic Ultrasound System, V5.0Sep 30, 2016