K-Jump Health Co., Ltd. - FDA 510(k) Cleared Devices
26
Total
26
Cleared
0
Denied
K-Jump Health Co., Ltd. has 26 FDA 510(k) cleared medical devices. Based in Mission Viejo, US.
Historical record: 26 cleared submissions from 1990 to 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by K-Jump Health Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by K-Jump Health Co., Ltd.
26 devices
Cleared
Sep 24, 2018
Probe Covers for Thermometers
General Hospital
189d
Cleared
Sep 28, 2017
Digital Thermometer
General Hospital
244d
Cleared
Aug 26, 2014
BASAL DIGITAL THERMOMETER
General Hospital
81d
Cleared
Mar 15, 2013
ULTRASONIC NEBULIZER (MESH TYPE)
Anesthesiology
297d
Cleared
Nov 19, 2012
NON-CONTACT THERMOMETER
General Hospital
256d
Cleared
Apr 04, 2011
DIGITAL FOREHEAD THERMOMETER
General Hospital
115d
Cleared
Feb 25, 2011
NON-CONTACT INFRARED THERMOMETER
General Hospital
144d
Cleared
Apr 09, 2010
PEAK EXPIRATORY FLOW METER, KN-9710
Anesthesiology
248d
Cleared
Oct 09, 2009
AUTO DIGITAL UPPER ARM BLOOD PRESSURE MONITOR, MODEL KP-7770
Cardiovascular
28d
Cleared
Jun 26, 2009
ULTRASONIC NEBULIZER SYSTEM, MODEL KN-9210
Anesthesiology
234d
Cleared
Jun 19, 2009
SMART-LOGIC AUTO DIGITAL UPPERARM BLOOD PRESSURE MONITOR, MODEL KP-7500,...
Cardiovascular
184d
Cleared
Jun 21, 2007
DIGITAL FOREHEAD THERMOMETER, MODEL# KD-2200
General Hospital
121d