510(k) K120668
K120668 is an FDA 510(k) premarket notification submitted by C-Rad Positioning AB for the device "SENTINEL". The FDA issued a decision of Substantially Equivalent on July 30, 2012. The device falls under product code IYE (Accelerator, Linear, Medical), a Class II device regulated under 21 CFR 892.5050. C-Rad Positioning AB has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 30, 2012
- Date Received
- March 5, 2012
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Accelerator, Linear, Medical
- Device Class
- Class II
- Regulation Number
- 892.5050
- Review Panel
- RA
- Submission Type