AccuFFRangio Plus— 510(k) K230303
Substantially EquivalentArteryFlow Technology Co., Ltd.
FDA 510(k) clearance K230303 for AccuFFRangio Plus, Substantially Equivalent on 2023-03-02. Applicant: ArteryFlow Technology Co., Ltd..
Clearance details
- Applicant
- ArteryFlow Technology Co., Ltd.
- Product code
- Code QHA
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Hangzhou City, CN
Data sourced from openFDA. This site is unofficial and independent of the FDA.