510(k) K962376
K962376 is an FDA 510(k) premarket notification submitted by Kreativ, Inc. for the device "KREATIV KURING LIGHT SYSTEM". The FDA issued a decision of Substantially Equivalent on March 21, 1997. The device falls under product code EBF (Material, Tooth Shade, Resin), a Class II device regulated under 21 CFR 872.3690. Kreativ, Inc. has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 21, 1997
- Date Received
- June 20, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Material, Tooth Shade, Resin
- Device Class
- Class II
- Regulation Number
- 872.3690
- Review Panel
- DE
- Submission Type