VERSABOARD, MODEL 7040


Device Classification Name

accelerator, linear, medical

510(k) Number K030051
Device Name VERSABOARD, MODEL 7040
Original Applicant
BIONIX DEVELOPMENT CORP.
5154 enterprise blvd.
toledo, 
OH 
43612

Original Contact james huttner
Regulation Number 892.5050
Classification Product Code
IYE  
Date Received 01/06/2003
Decision Date 04/04/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No