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U.S. Department of Health and Human Services

510(k) Premarket Notification
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101 to 110 of 483 Results
Applicant: BOSTON SCIENTIFIC CORP. Decision Date To: 04/18/2024
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Export all 483 Records to ExcelExport to Excel | Download Files | More About 510(k)
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modification to atlantis sr pro 2 and sr pro coronary imaging catheters, model 39014 and 38942 BOSTON SCIENTIFIC CORP. K063312 11/30/2006
occlusion balloon BOSTON SCIENTIFIC CORP. K062202 10/20/2006
maxforce tts single-use balloon dilator BOSTON SCIENTIFIC CORP. K061787 09/21/2006
wallflex enteral colonic stent with anchor lock delivery system BOSTON SCIENTIFIC CORP. K061877 09/15/2006
wellflex biliary rx stent system BOSTON SCIENTIFIC CORP. K061231 09/01/2006
filterwire ez embolic protection system (2.25 mm-3.5 mm) BOSTON SCIENTIFIC CORP. K061332 08/11/2006
sonicath ultra imaging catheter, 3.2f,20mhz models 37410/456221/c1020 BOSTON SCIENTIFIC CORP. K060947 04/19/2006
filterwire ez (2.25 mm - 3.5 mm) embolic protection system, models 20120-190, 20120-300 BOSTON SCIENTIFIC CORP. K051984 04/10/2006
isight imaging catheter, model 38986 BOSTON SCIENTIFIC CORP. K060175 03/24/2006
concerto bipolar needle electrode BOSTON SCIENTIFIC CORP. K060419 03/13/2006
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