510(k) K090706

ONCENTRA SIMULATION 2.3 by Nucletron Corporation — Product Code KPQ

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