510(k) K102259
K102259 is an FDA 510(k) premarket notification submitted by VATECH Co., Ltd. for the device "DENTAL COMPUTED TOMOGRAPHY X-RAY SYSTEM". The FDA issued a decision of Substantially Equivalent on Feb 18, 2011. The device falls under product code JAK (System, X-Ray, Tomography, Computed), a Class II device regulated under 21 CFR 892.1750. VATECH Co., Ltd. has 39 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 18, 2011
- Date Received
- Aug 10, 2010
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- System, X-Ray, Tomography, Computed
- Device Class
- Class II
- Regulation Number
- 892.1750
- Review Panel
- RA
- Submission Type
- 510(k)