510(k) K230259
K230259 is an FDA 510(k) premarket notification submitted by Shenzhen Up3D Technology Co., Ltd. for the device "Soreal Press, Soreal CAD". The FDA issued a decision of Substantially Equivalent on May 25, 2023. The device falls under product code EIH (Powder, Porcelain), a Class II device regulated under 21 CFR 872.6660.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 25, 2023
- Date Received
- Jan 31, 2023
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Powder, Porcelain
- Device Class
- Class II
- Regulation Number
- 872.6660
- Review Panel
- DE
- Submission Type
- 510(k)