PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50


Device Classification Name

accelerator, linear, medical

510(k) Number K010472
Device Name PATIENT DOSE VERIFICATION SYSTEM, MODEL TN-RD-50
Original Applicant
THOMSON & NIELSEN ELECTRONICS, LTD.
25b northside rd.
ottawa, ontario, 

CA

k2h 8s1

Original Contact andrew hartshorn
Regulation Number 892.5050
Classification Product Code
IYE  
Date Received 02/20/2001
Decision Date 05/08/2001
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

Type Traditional
Reviewed by Third Party No

Combination Product

No

Category: Uncategorized