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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 19 Results
ProductCode: DRF Applicant: BIOSENSE WEBSTER, INC. Decision Date To: 05/06/2024
 
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510(K)
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lassostar nav circular mapping catheter Biosense Webster, Inc. K211219 01/26/2022
lassostar circular mapping catheter Biosense Webster, Inc. K193632 06/30/2020
lasso nav duo loop catheter BIOSENSE WEBSTER, INC. K130602 08/14/2013
lasso 2515 nav eco variable catheter lasso nav eco catheter continued from line 2 BIOSENSE WEBSTER, INC. K113213 12/05/2011
webster duo-decapolar catheter BIOSENSE WEBSTER, INC. K101991 05/02/2011
webster cs catheter with ez steer technology, webster cs catheter with ez steer technology and auto id model: d-1263-04, BIOSENSE WEBSTER, INC. K101345 06/22/2010
lasso nav catheter BIOSENSE WEBSTER, INC. K093376 06/18/2010
coronary sinus deflectable mapping catheter, model d-1263-01, webster cs catheter with ez steer BIOSENSE WEBSTER, INC. K090898 09/04/2009
refstar plus with qwikpatch external reference patch, model d-1210-03, refstar plus cable, model m-4700-106 BIOSENSE WEBSTER, INC. K090120 03/24/2009
variable lasso nav catheter, models: d-1290-01, d-1290-02 BIOSENSE WEBSTER, INC. K081258 01/06/2009
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