510(k) K060330
K060330 is an FDA 510(k) premarket notification submitted by Ronvig Dental Mfg. A/S for the device "SEE-IT CARIES DETECTOR". The FDA issued a decision of Substantially Equivalent on April 7, 2006. The device falls under product code LFC (Device, Caries Detection), a Class II device regulated under 21 CFR 872.1740.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 7, 2006
- Date Received
- February 9, 2006
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, Caries Detection
- Device Class
- Class II
- Regulation Number
- 872.1740
- Review Panel
- DE
- Submission Type