CLEARVISION


Device Classification Name

system,x-ray,extraoral source,digital

510(k) Number K112380
Device Name CLEARVISION
Applicant
MIDMARK CORP.
675 heathrow drive
lincolnshire, 
IL 
60069

Applicant Contact lisa bartakovics
Correspondent
MIDMARK CORP.
675 heathrow drive
lincolnshire, 
IL 
60069

Correspodent Contact lisa bartakovics
Regulation Number 872.1800
Classification Product Code
MUH  
Date Received 08/17/2011
Decision Date 11/22/2011
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Dental

510k Review Panel

Radiology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No