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

uPMR 790

K Number: K192672 · Decision Nov 20, 2019
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
13
Applicant Total
83
Review Days
55

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Basic Information

Device Name
uPMR 790
K Number
K192672
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1200
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shanghai United Imaging Healthcare Co., Ltd.
Date Received
September 26, 2019
Decision Date
November 20, 2019
Product Code
OUO
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
OUO Tomographic Imager Combining Emission Computed Tomography With Nuclear Magnetic Resonance

Similar 510(k) Clearances

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Other Clearances by Shanghai United Imaging Healthcare Co., Ltd.

K Number Device Name
K260113 uMR Astra
K253077 uOmnispace.MR
K260524 uMI Panvivo (uMI Panvivo LS); uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX); uMI Panvivo (uMI Panvivo ES)
K253564 uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX); uMI Panvivo (uMI Panvivo ES)
K253173 uCT 780 with uWS-CT-Dual Energy Analysis
K252000 uDR Arria & uDR Aris
K252371 uMR 680
K250045 uWS-Angio Pro
K251167 uDR Aurora CX
K250040 uWS-Angio
Search all 83 clearances from Shanghai United Imaging Healthcare Co., Ltd. →