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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name System, Image Processing, Radiological
510(k) Number K022585
Device Name KIMAX QMA
Applicant
Medical Metrics, Inc.
10540 Rockely Rd.
Suite 200
Houston,  TX  77099
Applicant Contact MARK LAMP
Correspondent
Medical Metrics, Inc.
10540 Rockely Rd.
Suite 200
Houston,  TX  77099
Correspondent Contact MARK LAMP
Regulation Number892.2050
Classification Product Code
LLZ  
Date Received08/05/2002
Decision Date 10/11/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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