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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name System, Digital Image Communications, Radiological
510(k) Number K900227
Device Name MVP (MULTI-VENDOR PROTOCOL CONVERTOR)
Applicant
Merge Technologies, Inc.
P.O. Box 27366
Milwaukee,  WI  53227
Applicant Contact CAROL J GRACZYK
Correspondent
Merge Technologies, Inc.
P.O. Box 27366
Milwaukee,  WI  53227
Correspondent Contact CAROL J GRACZYK
Regulation Number892.2020
Classification Product Code
LMD  
Date Received01/17/1990
Decision Date 02/12/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
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