FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Wireless Intelligent Thermometer

K Number: K182437 · Decision May 5, 2019
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
10
Review Days
240

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Basic Information

Device Name
Wireless Intelligent Thermometer
K Number
K182437
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Shenzhen Jumper Medical Equipment Co., Ltd.
Date Received
September 7, 2018
Decision Date
May 5, 2019
Product Code
FLL
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FLL Continuous Measurement Thermometer

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K Number Device Name
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K140582 FINGERTIP PULSE OXIMETER
K131457 FETAL ULTRASONIC MONITOR AND ACCESSORIES
K131243 NON-CONTACT INFRARED THERMOMETER
K110124 FETAL DOPPLER JPD-100S