KLARITY


Device Classification Name

accelerator, linear, medical

510(k) Number K022708
Device Name KLARITY
Original Applicant
LARSON PRODUCTS, INC.
2844 banwick rd.
columbus, 
OH 
43232 -2115

Original Contact peter m larson
Regulation Number 892.5050
Classification Product Code
IYE  
Date Received 08/14/2002
Decision Date 11/12/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No