Cleveland Medical Devices, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Cleveland Medical Devices, Inc. has 8 FDA 510(k) cleared medical devices. Based in Cleveland, US.
Historical record: 8 cleared submissions from 1995 to 2007. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Cleveland Medical Devices, Inc. Filter by specialty or product code using the sidebar.
8 devices
Cleared
Apr 06, 2007
KINESIA
Neurology
98d
Cleared
Nov 17, 2004
FAMILY OF CRYSTAL 20 MONITORS MODEL #CS20-600,900,1300,1400,2400 & 120
Neurology
111d
Cleared
Feb 19, 2002
CRYSTAL MONITOR MODEL 16
Neurology
90d
Cleared
Jul 05, 2000
CRYSTAL-EEG MODEL 15
Neurology
90d
Cleared
May 22, 1997
CRYSTAL-EEG MODEL 10 (MODEL 10)
Neurology
87d
Cleared
Mar 21, 1997
LIBERTY VALVE
Gastroenterology & Urology
119d
Cleared
Dec 04, 1996
FOOT WEIGHT ALARM
Physical Medicine
155d
Cleared
Oct 30, 1995
PRESSORE MONITOR
Physical Medicine
20d