510(k) K070523
K070523 is an FDA 510(k) premarket notification submitted by Led Dental, Inc. for the device "MODIFICATION TO: VELSCOPE". The FDA issued a decision of Substantially Equivalent on April 5, 2007. The device falls under product code NXV (Diagnostic Light, Soft Tissue Detector), a Class II device regulated under 21 CFR 872.6350. Led Dental, Inc. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 5, 2007
- Date Received
- February 23, 2007
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Diagnostic Light, Soft Tissue Detector
- Device Class
- Class II
- Regulation Number
- 872.6350
- Review Panel
- DE
- Submission Type
To be used as an aid in the detection or visualization of abnormalities of intraoral soft tissue. An adjunct to traditional intraoral examination by incandescent light to enhance the visualization of oral mucosal abnormalities