510(k) K113672
K113672 is an FDA 510(k) premarket notification submitted by VATECH Co., Ltd. for the device "PCH-2500 DIGITAL EXTRAORAL SOURCE X-RAY SYSTEM". The FDA issued a decision of Substantially Equivalent on Mar 27, 2012. The device falls under product code MUH (System, X-Ray, Extraoral Source, Digital), a Class II device regulated under 21 CFR 872.1800. VATECH Co., Ltd. has 39 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 27, 2012
- Date Received
- Dec 13, 2011
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- System, X-Ray, Extraoral Source, Digital
- Device Class
- Class II
- Regulation Number
- 872.1800
- Review Panel
- RA
- Submission Type
- 510(k)