MODIFICATION TO MEDIPRIME


Device Classification Name

system, image processing, radiological

510(k) Number K023936
Device Name MODIFICATION TO MEDIPRIME
Original Applicant
ALGOTEC SYSTEMS, LTD.
p.o. box 6718
efrat, 

IL

90435

Original Contact eli m orbach
Regulation Number 892.2050
Classification Product Code
LLZ  
Date Received 11/26/2002
Decision Date 12/20/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No