510(k) K182009
K182009 is an FDA 510(k) premarket notification submitted by DiaDent Group International for the device "Dia-Proseal". The FDA issued a decision of Substantially Equivalent on Sep 26, 2019. 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 23 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 26, 2019
- Date Received
- Jul 27, 2018
- Clearance Type
- Traditional
- 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
- 510(k)