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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 21 Results
ProductCode: IYN Applicant: TOSHIBA MEDICAL SYSTEMS CORPORATION Decision Date To: 02/22/2017
 
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Export all 21 Records to ExcelExport to Excel | Download Files | More About 510(k)
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aplio 500/400/300 diagnostic ultrasound system v4.0 TOSHIBA MEDICAL SYSTEMS CORPORATION K133761 04/22/2014
aplio 500/400/300 diagnostic ultrasound system v6.0 TOSHIBA MEDICAL SYSTEMS CORPORATION K151451 07/09/2015
aplio 500/400/300 diagnostic ultrasound system, v5.0 TOSHIBA MEDICAL SYSTEMS CORPORATION K141459 10/28/2014
aplio 500/400/300 v3.0 TOSHIBA MEDICAL SYSTEMS CORPORATION K123992 02/06/2013
aplio i900/i800/i700 diagnostic ultrasound system, v2.0 TOSHIBA MEDICAL SYSTEMS CORPORATION K161843 09/21/2016
aplio i900/i800/i700 diagnostic ultrasound system, v2.1 TOSHIBA MEDICAL SYSTEMS CORPORATION K163702 05/30/2017
aplio i900/i800/i700/i600 diagnostic ultrasound system, v2.4 Toshiba Medical Systems Corporation K173090 01/11/2018
aplio xg diagnostic ultrasound system, model ssa-790a, version 1.0 TOSHIBA MEDICAL SYSTEMS CORPORATION K063130 11/02/2006
model ssa-680a xario xg diagnostic ultrasound system, version 1.00 TOSHIBA MEDICAL SYSTEMS CORPORATION K072918 10/29/2007
ssa-770a, aplio version 5.5 TOSHIBA MEDICAL SYSTEMS CORPORATION K041499 06/10/2004
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