SPOT PRO (220V), MODEL 131.099


Device Classification Name

system,planning,radiation therapy treatment

510(k) Number K022741
Device Name SPOT PRO (220V), MODEL 131.099
Original Applicant
NUCLETRON CORPORATION
7080 columbia gateway dr.
columbia, 
MD 
21046 -2133

Original Contact lisa dimmick
Regulation Number 892.5050
Classification Product Code
MUJ  
Date Received 08/19/2002
Decision Date 10/24/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No