510(k) K232952
K232952 is an FDA 510(k) premarket notification submitted by Whitepeaks Dental Solutions GmbH for the device "Copran Zri". The FDA issued a decision of Substantially Equivalent on June 24, 2024. The device falls under product code EIH (Powder, Porcelain), a Class II device regulated under 21 CFR 872.6660. Whitepeaks Dental Solutions GmbH has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 24, 2024
- Date Received
- September 21, 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