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

uMR 680

K Number: K222755 · Decision Feb 16, 2023
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
4
Review Days
157

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Basic Information

Device Name
uMR 680
K Number
K222755
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shanghai United Imaging Intelligence Co., Ltd.
Date Received
September 12, 2022
Decision Date
February 16, 2023
Product Code
LNH
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
LNH System, Nuclear Magnetic Resonance Imaging

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