K-Jump Health Co., Ltd. - FDA 510(k) Cleared Devices
26
Total
26
Cleared
0
Denied
FDA 510(k) cleared devices by K-Jump Health Co., Ltd. Cardiovascular ✕
8 devices
Cleared
Oct 09, 2009
AUTO DIGITAL UPPER ARM BLOOD PRESSURE MONITOR, MODEL KP-7770
Cardiovascular
28d
Cleared
Jun 19, 2009
SMART-LOGIC AUTO DIGITAL UPPERARM BLOOD PRESSURE MONITOR, MODEL KP-7500,...
Cardiovascular
184d
Cleared
Aug 14, 2006
ARM BLOOD PRESSURE MONITOR, MODEL KP-7600
Cardiovascular
53d
Cleared
Apr 21, 2005
MODIFICATION TO ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822
Cardiovascular
121d
Cleared
Sep 09, 2003
BLOOD PRESSURE MONITOR, MODEL KP-7000
Cardiovascular
28d
Cleared
Nov 21, 2002
BLOOD PRESSURE MONITOR SMARTLOGIC, MODELS KP-6210 AND KP-6211
Cardiovascular
79d
Cleared
Mar 05, 2002
ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822
Cardiovascular
74d
Cleared
Mar 19, 2001
WRISTWATCH BPM BLOOD PRESSURE MONITOR, MODEL KP-6120
Cardiovascular
206d