ILUMA VISION


Device Classification Name

system, image processing, radiological

510(k) Number K081347
Device Name ILUMA VISION
Applicant
IMTEC CORP.
2401 north commerce
ardmore, 
OK 
73401

Applicant Contact brad vance
Regulation Number 892.2050
Classification Product Code
LLZ  
Date Received 05/14/2008
Decision Date 05/28/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

statement

statement

Type Traditional
Reviewed by Third Party Yes

Combination Product

No

Recalls CDRH Recalls