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

Infrared Thermometer

K Number: K211752 · Decision Jan 21, 2022
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
14
Review Days
228

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Basic Information

Device Name
Infrared Thermometer
K Number
K211752
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Beijing Choice Electronic Technology Co., Ltd.
Date Received
June 7, 2021
Decision Date
January 21, 2022
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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K181503 Fingertip Pulse Oximeter
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