510(k) K052263
K052263 is an FDA 510(k) premarket notification submitted by Cosmedent, Inc. for the device "MULTIPLE (TOOTH DESENSITIZER)". The FDA issued a decision of Substantially Equivalent on Dec 16, 2005. The device falls under product code LBH (Varnish, Cavity), a Class II device regulated under 21 CFR 872.3260. Cosmedent, Inc. has 27 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 16, 2005
- Date Received
- Aug 19, 2005
- 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)