Fluke Biomedical is one of 5297 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fluke Biomedical - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Fluke Biomedical has 6 FDA 510(k) cleared medical devices. Based in Orange, US.
Historical record: 6 cleared submissions from 2008 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Fluke Biomedical Filter by specialty or product code using the sidebar.
Fluke Biomedical — FDA 510(k) Products and Clearance History
6 devices
Cleared
Jan 25, 2013
ESA615
Cardiovascular
213d
Cleared
Oct 11, 2012
ESA620 ELECTRICAL SAFETY ANALYZER
Cardiovascular
121d
Cleared
Sep 02, 2011
PROSIM 4, PROSIM 6, PROSIM 8
Cardiovascular
199d
Cleared
Apr 13, 2011
MPS450 MULTIPARAMETER SIMULATOR
Cardiovascular
149d
Cleared
Dec 24, 2008
IMPULSE 7010 DEFIBRILLATOR SELECTABLE LOADS
Cardiovascular
41d
Cleared
Jan 28, 2008
IMPULSE 6000D/7000DP
Cardiovascular
180d