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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