510(k) K100172
K100172 is an FDA 510(k) premarket notification submitted by Tokuyama Dental Corporation for the device "TOKUYAMA SHIELD FORCE". The FDA issued a decision of Substantially Equivalent on Oct 21, 2010. The device falls under product code LBH (Varnish, Cavity), a Class II device regulated under 21 CFR 872.3260. Tokuyama Dental Corporation has 18 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 21, 2010
- Date Received
- Jan 21, 2010
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Varnish, Cavity
- Device Class
- Class II
- Regulation Number
- 872.3260
- Review Panel
- DE
- Submission Type
- 510(k)