510(k) K081405
K081405 is an FDA 510(k) premarket notification submitted by Doxa Dental AB for the device "XERACEM". The FDA issued a decision of Substantially Equivalent on Aug 21, 2008. The device falls under product code EMA (Cement, Dental), a Class II device regulated under 21 CFR 872.3275. Doxa Dental AB has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 21, 2008
- Date Received
- May 19, 2008
- Clearance Type
- Abbreviated
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cement, Dental
- Device Class
- Class II
- Regulation Number
- 872.3275
- Review Panel
- DE
- Submission Type
- 510(k)