Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

K-Jump Health Co., Ltd. · Predicate Candidate Screening

26 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

115 daysmedian FDA review time

256 days90th percentile

26clearances measured

K-number	Device	Applicant	Decided	Review days	Recalls (K-match)
K180714	Probe Covers for Thermometers	K-Jump Health Co., Ltd.	2018-09-24	189	0
K170262	Digital Thermometer	K-Jump Health Co., Ltd.	2017-09-28	244	0
K141505	BASAL DIGITAL THERMOMETER	K-Jump Health Co., Ltd.	2014-08-26	81	0
K121520	ULTRASONIC NEBULIZER (MESH TYPE)	K-Jump Health Co., Ltd.	2013-03-15	297	0
K120711	NON-CONTACT THERMOMETER	K-Jump Health Co., Ltd.	2012-11-19	256	0
K103617	DIGITAL FOREHEAD THERMOMETER	K-Jump Health Co., Ltd.	2011-04-04	115	1
K102947	NON-CONTACT INFRARED THERMOMETER	K-Jump Health Co., Ltd.	2011-02-25	144	0
K092335	PEAK EXPIRATORY FLOW METER, KN-9710	K-Jump Health Co., Ltd.	2010-04-09	248	0
K092806	AUTO DIGITAL UPPER ARM BLOOD PRESSURE MONITOR, MODEL KP-7770	K-Jump Health Co., Ltd.	2009-10-09	28	0
K083256	ULTRASONIC NEBULIZER SYSTEM, MODEL KN-9210	K-Jump Health Co., Ltd.	2009-06-26	234	0
K083753	SMART-LOGIC AUTO DIGITAL UPPERARM BLOOD PRESSURE MONITOR, MO	K-Jump Health Co., Ltd.	2009-06-19	184	0
K070491	DIGITAL FOREHEAD THERMOMETER, MODEL# KD-2200	K-Jump Health Co., Ltd.	2007-06-21	121	0
K061760	ARM BLOOD PRESSURE MONITOR, MODEL KP-7600	K-Jump Health Co., Ltd.	2006-08-14	53	0
K060240	K-JUMP DIGITAL THERMOMETER WITH BATTERY-LESS PATCH, MODEL KD	K-Jump Health Co., Ltd.	2006-05-19	108	0
K051365	COMPRESSOR NEBULIZER SYSTEM, MODEL KN-9321	K-Jump Health Co., Ltd.	2005-07-22	58	0
K043531	MODIFICATION TO ARM BLOOD PRESSURE MONITOR, MODELS KP-6821,	K-Jump Health Co., Ltd.	2005-04-21	121	0
K032492	BLOOD PRESSURE MONITOR, MODEL KP-7000	K-Jump Health Co., Ltd.	2003-09-09	28	0
K022916	BLOOD PRESSURE MONITOR SMARTLOGIC, MODELS KP-6210 AND KP-621	K-Jump Health Co., Ltd.	2002-11-21	79	0
K021851	DIGITAL CLINICAL THERMOMETER, MODEL KD-193	K-Jump Health Co., Ltd.	2002-07-17	42	0
K014204	ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822	K-Jump Health Co., Ltd.	2002-03-05	74	0
K002665	WRISTWATCH BPM BLOOD PRESSURE MONITOR, MODEL KP-6120	K-Jump Health Co., Ltd.	2001-03-19	206	0
K984551	INFRARED EAR THERMOMETER, MODEL KI-8120	K-Jump Health Co., Ltd.	2000-01-14	388	0
K984553	TALKING DIGITAL THERMOMETER, MODEL KV-171	K-Jump Health Co., Ltd.	1999-01-14	23	0
K981456	BABY PACIFIER DIGITAL THERMOMETER	K-Jump Health Co., Ltd.	1998-07-02	70	0
K974195	FLEXIBLE TIP DIGITAL THERMOMETER	K-Jump Health Co., Ltd.	1998-02-04	89	0
K903590	KEJUMP DIGITAL CLINICAL THERMOMETER	K-Jump Health Co., Ltd.	1990-10-22	75	0

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda