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K-Jump Health Co., Ltd.

New Taipei City, TW

K-JUMP HEALTH CO., LTD. appears in FDA device records in New Taipei City, TW. FDA records list 26 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
26
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 26 510(k) clearances for K-Jump Health Co., Ltd. between 1990 and 2018. The busiest year on record is 2002, with 3. The most recent is 2018, with 1.

Clearances by year, as a table
510(k) clearance decisions for K-Jump Health Co., Ltd., by decision year
YearClearances
19901
19982
19991
20001
20011
20023
20031
20052
20062
20071
20093
20101
20112
20121
20131
20141
20171
20181
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K180714Probe Covers for ThermometersFLLSubstantially Equivalent
K170262Digital ThermometerFLLSubstantially Equivalent
K141505BASAL DIGITAL THERMOMETERFLLSubstantially Equivalent
K121520ULTRASONIC NEBULIZER (MESH TYPE)CAFSubstantially Equivalent
K120711NON-CONTACT THERMOMETERFLLSubstantially Equivalent
K103617DIGITAL FOREHEAD THERMOMETERFLLSubstantially Equivalent
K102947NON-CONTACT INFRARED THERMOMETERFLLSubstantially Equivalent
K092335PEAK EXPIRATORY FLOW METER, KN-9710BZHSubstantially Equivalent
K092806AUTO DIGITAL UPPER ARM BLOOD PRESSURE MONITOR, MODEL KP-7770DXNSubstantially Equivalent
K083256ULTRASONIC NEBULIZER SYSTEM, MODEL KN-9210CAFSubstantially Equivalent
K083753SMART-LOGIC AUTO DIGITAL UPPERARM BLOOD PRESSURE MONITOR, MODEL KP-7500, FULLY FUZZY AUTO DIGITAL UPPER ARM BLOOD PRESSUDXNSubstantially Equivalent
K070491DIGITAL FOREHEAD THERMOMETER, MODEL# KD-2200FLLSubstantially Equivalent
K061760ARM BLOOD PRESSURE MONITOR, MODEL KP-7600DXNSubstantially Equivalent
K060240K-JUMP DIGITAL THERMOMETER WITH BATTERY-LESS PATCH, MODEL KD-2100FLLSubstantially Equivalent
K051365COMPRESSOR NEBULIZER SYSTEM, MODEL KN-9321CAFSubstantially Equivalent
K043531MODIFICATION TO ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822DXNSubstantially Equivalent
K032492BLOOD PRESSURE MONITOR, MODEL KP-7000DXNSubstantially Equivalent
K022916BLOOD PRESSURE MONITOR SMARTLOGIC, MODELS KP-6210 AND KP-6211DXNSubstantially Equivalent
K021851DIGITAL CLINICAL THERMOMETER, MODEL KD-193FLLSubstantially Equivalent
K014204ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822DXNSubstantially Equivalent
K002665WRISTWATCH BPM BLOOD PRESSURE MONITOR, MODEL KP-6120DXNSubstantially Equivalent
K984551INFRARED EAR THERMOMETER, MODEL KI-8120FLLSubstantially Equivalent
K984553TALKING DIGITAL THERMOMETER, MODEL KV-171FLLSubstantially Equivalent
K981456BABY PACIFIER DIGITAL THERMOMETERFLLSubstantially Equivalent
K974195FLEXIBLE TIP DIGITAL THERMOMETERFLLSubstantially Equivalent
K903590KEJUMP DIGITAL CLINICAL THERMOMETERFLLSubstantially Equivalent

Registered establishments

FDA registered establishments for K-Jump Health Co., Ltd., with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
80435103003335291K-JUMP HEALTH CO., LTD.No 56, Wu Kung 5th Rd., New Taipei City 24890 TW2026

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain