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Parker Quality & Compliance

PQC Reg Watch

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510(k) clearance

uAngio AVIVA CX

FDA 510(k) source

510(k) number
K253726
Applicant
Shanghai United Imaging Healthcare Co., Ltd.
Decision date
Aug 21, 2026
Date received
Nov 24, 2025
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
OWB
Device type
Interventional Fluoroscopic X-Ray System
Device class
Class II
Regulation
21 CFR 892.1650
Advisory committee
Radiology
Statement or summary
Summary
Third party
N
Location
Shanghai, CN