510(k) K210333
K210333 is an FDA 510(k) premarket notification submitted by DiaDent Group International for the device "DiaPaste". The FDA issued a decision of Substantially Equivalent on March 25, 2021. The device falls under product code KIF (Resin, Root Canal Filling), a Class II device regulated under 21 CFR 872.3820. DiaDent Group International has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 25, 2021
- Date Received
- February 5, 2021
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Resin, Root Canal Filling
- Device Class
- Class II
- Regulation Number
- 872.3820
- Review Panel
- DE
- Submission Type