AccuFFRangio— 510(k) K210093
Substantially EquivalentArteryFlow Technology Co., Ltd.
FDA 510(k) clearance K210093 for AccuFFRangio, Substantially Equivalent on 2021-09-10. Applicant: ArteryFlow Technology Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- ArteryFlow Technology Co., Ltd.
- Product code
- Code QHA
- Device class
- Class 2
- Regulation
- 21 CFR 892.1600
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hangzhou City, CN
Recent devices under product code QHA
view allMore clearances from ArteryFlow Technology Co., Ltd.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.