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K-Jump Health Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
26
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K180714Probe Covers for ThermometersSeptember 24, 2018
K170262Digital ThermometerSeptember 28, 2017
K141505BASAL DIGITAL THERMOMETERAugust 26, 2014
K121520ULTRASONIC NEBULIZER (MESH TYPE)March 15, 2013
K120711NON-CONTACT THERMOMETERNovember 19, 2012
K103617DIGITAL FOREHEAD THERMOMETERApril 4, 2011
K102947NON-CONTACT INFRARED THERMOMETERFebruary 25, 2011
K092335PEAK EXPIRATORY FLOW METER, KN-9710April 9, 2010
K092806AUTO DIGITAL UPPER ARM BLOOD PRESSURE MONITOR, MODEL KP-7770October 9, 2009
K083256ULTRASONIC NEBULIZER SYSTEM, MODEL KN-9210June 26, 2009
K083753SMART-LOGIC AUTO DIGITAL UPPERARM BLOOD PRESSURE MONITOR, MODEL KP-7500, FULLY FUZZY AUTO DIGITAL UPJune 19, 2009
K070491DIGITAL FOREHEAD THERMOMETER, MODEL# KD-2200June 21, 2007
K061760ARM BLOOD PRESSURE MONITOR, MODEL KP-7600August 14, 2006
K060240K-JUMP DIGITAL THERMOMETER WITH BATTERY-LESS PATCH, MODEL KD-2100May 19, 2006
K051365COMPRESSOR NEBULIZER SYSTEM, MODEL KN-9321July 22, 2005
K043531MODIFICATION TO ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822April 21, 2005
K032492BLOOD PRESSURE MONITOR, MODEL KP-7000September 9, 2003
K022916BLOOD PRESSURE MONITOR SMARTLOGIC, MODELS KP-6210 AND KP-6211November 21, 2002
K021851DIGITAL CLINICAL THERMOMETER, MODEL KD-193July 17, 2002
K014204ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822March 5, 2002