510(k) K151707
K151707 is an FDA 510(k) premarket notification submitted by Rayence Co., Ltd. for the device "EzSensor Soft, EzSensor Soft i, EzSensor Bio, and EzSensor Bio i". The FDA issued a decision of Substantially Equivalent on Jul 19, 2015. The device falls under product code MUH (System, X-Ray, Extraoral Source, Digital), a Class II device regulated under 21 CFR 872.1800. Rayence Co., Ltd. has 38 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jul 19, 2015
- Date Received
- Jun 24, 2015
- Clearance Type
- Special
- 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)