FDA 510(k) Applications Submitted by Doug Blakely

FDA 510(k) Number Submission Date Device Name Applicant
K150030 01/08/2015 Fukuda Denshi DynaScope Model DS-8000 Series Patient Monitor Fukuda Denshi USA, Inc.
K131973 06/28/2013 UNEXEF-38G ULTRASOUND SYSTEM TOYOTA TSUSHO CORPORATION
K112521 08/31/2011 FUKUDA DENSHI VASERA MODEL VS-1500 FUKUDA DENSHI USA, INC.
K173226 10/03/2017 CardiMax Electrocardiograph Fukuda Denshi USA, Inc.
K072919 10/15/2007 VENDYS, MODEL 6000 B B/C ENDOTHELIX, INC.
K103134 10/25/2010 FUKUDA DENSHI FUKUDA DENSHI USA, INC.
K083697 12/15/2008 FUKUDA DENSHI DYNASCOPE MODEL DS-7000 SERIES PATIENT MONITOR, MODEL DS-7000//7000M/7210/7210M FUKUDA DENSHI USA, INC.
K134046 12/31/2013 FUKUDA DENSHI DYNASCOPE MODEL DS-8100N/8100M PATIENT MONITOR FUKUDA DENSHI USA, INC.
K060980 04/10/2006 VENDYS MODEL 5000 B/BC ENDOTHELIX, INC.


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