OMNIVISION


Device Classification Name

system, image processing, radiological

510(k) Number K110040
Device Name OMNIVISION
Applicant
MODERN MODULE INC
425 cheongchun-dong,
bupyung-ku
lncheon, 

KR

Applicant Contact samuel koh
Regulation Number 892.2050
Classification Product Code
LLZ  
Date Received 01/06/2011
Decision Date 01/26/2011
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

summary

summary

Type Traditional
Reviewed by Third Party Yes

Combination Product

No