510(k) K113406
K113406 is an FDA 510(k) premarket notification submitted by Dentsply International, Inc. for the device "AQUASIL ULTRA SMART WETTING IMPRESSION MATERIAL". The FDA issued a decision of Substantially Equivalent on February 13, 2012. The device falls under product code ELW (Material, Impression), a Class II device regulated under 21 CFR 872.3660. Dentsply International, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 13, 2012
- Date Received
- November 18, 2011
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Material, Impression
- Device Class
- Class II
- Regulation Number
- 872.3660
- Review Panel
- DE
- Submission Type