510(k) K090706
K090706 is an FDA 510(k) premarket notification submitted by Nucletron Corporation for the device "ONCENTRA SIMULATION 2.3". The FDA issued a decision of Substantially Equivalent on June 15, 2009. The device falls under product code KPQ (System, Simulation, Radiation Therapy), a Class II device regulated under 21 CFR 892.5840. Nucletron Corporation has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 15, 2009
- Date Received
- March 17, 2009
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Simulation, Radiation Therapy
- Device Class
- Class II
- Regulation Number
- 892.5840
- Review Panel
- RA
- Submission Type