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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name filter, intravascular, cardiovascular
510(k) Number K951508
Device Name STAINLESS STEEL GREENFIELD VENA CAVA FILTER WITH 24F INTRODUCER SYSTEM
Original Applicant
BOSTON SCIENTIFIC CORP.
480 pleasant st.
watertown,  MA  02472 -2407
Original Contact laura mondano
Regulation Number870.3375
Classification Product Code
DTK  
Date Received04/03/1995
Decision Date 06/22/1995
Decision substantially equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
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