Devices · Shanghai United Imaging Healthcare Co.,Ltd.
uAngio AVIVA CX
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
- 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