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

Infrared Body Thermometer

K Number: K200781 · Decision Dec 9, 2020
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
1
Review Days
273

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Basic Information

Device Name
Infrared Body Thermometer
K Number
K200781
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Heitaida Technology Co., Ltd.
Date Received
March 11, 2020
Decision Date
December 9, 2020
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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