FDA 510(k) Applications Submitted by Toshiba Medical Systems Corporation, Japan
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K121577 |
05/30/2012 |
APLIO ARTIDA DIAGNOSTIC ULTRASOUND SYSTEM |
TOSHIBA MEDICAL SYSTEMS CORPORATION, JAPAN |
| K120546 |
02/23/2012 |
AQUILION PREMIUM |
TOSHIBA MEDICAL SYSTEMS CORPORATION, JAPAN |
| K121910 |
06/29/2012 |
OCTAVE SPEEDER HEAD |
TOSHIBA MEDICAL SYSTEMS CORPORATION, JAPAN |
| K121911 |
06/29/2012 |
OCTAVE SPEEDER SPINE |
TOSHIBA MEDICAL SYSTEMS CORPORATION, JAPAN |
| K112054 |
07/19/2011 |
INFINIX CF-I/SP AND INFINIX VF-I/SP MODEL INFX-8000V |
TOSHIBA MEDICAL SYSTEMS CORPORATION, JAPAN |
| K102489 |
08/31/2010 |
VANTAGE TITAN 3T |
TOSHIBA MEDICAL SYSTEMS CORPORATION, JAPAN |
| K172878 |
09/21/2017 |
Vantage Titan 3T, MRT-3010/A7, M-Power GX |
Toshiba Medical Systems Corporation, Japan |
| K133324 |
10/29/2013 |
SURESUBTRACTION LUNG |
TOSHIBA MEDICAL SYSTEMS CORPORATION, JAPAN |
| K103645 |
12/13/2010 |
APLIO XG DIAGNOSTIC ULTRASOUND SYSTEM |
TOSHIBA MEDICAL SYSTEMS CORPORATION, JAPAN |
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