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

InferRead Lung CT.AI

K Number: K192880 · Decision Jul 2, 2020
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
19
Applicant Total
1
Review Days
267

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Basic Information

Device Name
InferRead Lung CT.AI
K Number
K192880
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Beijing Infervision Technology Co., Ltd.
Date Received
October 9, 2019
Decision Date
July 2, 2020
Product Code
OEB
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
OEB Lung Computed Tomography System, Computer-Aided Detection

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