Cleared Traditional

uPMR 790

K222540 · Shanghai United Imaging Healthcare Co., Ltd. · Radiology

Nov 2022

Decision

84d

Days

Class 2

Risk

About This 510(k) Submission

K222540 is an FDA 510(k) clearance for the uPMR 790, a Tomographic Imager Combining Emission Computed Tomography With Nuclear Magnetic Resonance (Class II — Special Controls, product code OUO), submitted by Shanghai United Imaging Healthcare Co., Ltd. (Shanghai, CN). The FDA issued a Cleared decision on November 14, 2022, 84 days after receiving the submission on August 22, 2022. This device falls under the Radiology review panel. Regulated under 21 CFR 892.1200.

Submission Details

510(k) Number	K222540 FDA.gov
FDA Decision	Cleared SESE
Date Received	August 22, 2022
Decision Date	November 14, 2022
Days to Decision	84 days
Submission Type	Traditional
Review Panel	Radiology (RA)
Summary	Summary PDF

Device Classification

Product Code	OUO — Tomographic Imager Combining Emission Computed Tomography With Nuclear Magnetic Resonance
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 892.1200
Definition	Imager That Generates Both Both Magnetic Resonance (mr) And Positron Emission Tomography (pet) Images And Provides Registration And Fusion Of These Images. Pet And Mr Images Can Be Acquired Either Simultaneously Or Sequentially. Anatomical Mr Images Are Used For Pet Attenuation Correction.