510(k) K992751

SOMAVISION by Varian Assoc., Inc. — Product Code KPQ

K992751 is an FDA 510(k) premarket notification submitted by Varian Assoc., Inc. for the device "SOMAVISION". The FDA issued a decision of Substantially Equivalent on February 16, 2000. The device falls under product code KPQ (System, Simulation, Radiation Therapy), a Class II device regulated under 21 CFR 892.5840. Varian Assoc., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 16, 2000
Date Received
August 16, 1999
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