AccuContour— 510(k) K221706
Substantially EquivalentManteia Technologies Co., Ltd.
FDA 510(k) clearance K221706 for AccuContour, Substantially Equivalent on 2023-03-09. Applicant: Manteia Technologies Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Manteia Technologies Co., Ltd.
- Product code
- Code QKB
- Device class
- Class 2
- Regulation
- 21 CFR 892.2050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Xiamen, CN
Recent devices under product code QKB
view allMore clearances from Manteia Technologies Co., Ltd.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.