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Devices · Shanghai United Imaging Healthcare Co.,Ltd.

uAngio AVIVA CX

510(k)K243376RadiologyOWB

Shanghai United Imaging Healthcare Co.,Ltd. is listed for uAngio AVIVA CX (K243376). The FDA list gives April 28, 2025 as the date of the final decision. The lead panel is Radiology, and the database link on the FDA list is the 510(k) pathway. openFDA describes product code OWB as “Interventional Fluoroscopic X-Ray System”: Interventional fluoroscopy openFDA records this submission’s decision description as “Substantially Equivalent.” This paragraph is assembled only from those public fields. It is not an FDA review, not a determination of safety or effectiveness, and not medical advice. Official record: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K243376

Official FDA database record

Date of final decision
April 28, 2025
Company on the FDA list
Shanghai United Imaging Healthcare Co.,Ltd.
Lead panel
Radiology
Primary product code
OWB
openFDA device name for the code
Interventional Fluoroscopic X-Ray System
Device class
2
Regulation number
892.1650
openFDA decision description
Substantially Equivalent
openFDA decision code
SESE
Statement or summary label
Summary

Product-code text from openFDA

Interventional fluoroscopy

Other listings for this company