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

Infrared Thermometer

K Number: K201980 · Decision Dec 18, 2020
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
12
Review Days
155

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Basic Information

Device Name
Infrared Thermometer
K Number
K201980
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Contec Medical Systems Co.,Ltd
Date Received
July 16, 2020
Decision Date
December 18, 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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K Number Device Name
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K232908 Color Doppler Ultrasound Diagnostic System (CMS1700B), Color Doppler Ultrasound Diagnostic System (CMS1700C)
K220245 Pocket Fetal Doppler (Models CONTEC10C and CONTEC10CL)
K202757 CONTEC08A Electronic Sphygmomanometer, CONTEC08C Electronic Sphygmomanometer, ABPM50 Automatic Blood Pressure Monitor
K171360 CONTEC™ Electrocardiograph
K170856 CMS600P2 B-Ultrasound Diagnostic System
K170954 Portable ECG Monitor
K152863 Portable ECG Monitor
K141362 PULSE OXIMETER CMS50EW
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