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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Display, Cathode-Ray Tube, Medical
510(k) Number K934093
Device Name 580CDR DISPLAY DRIVER
Applicant
Vidco, Inc.
6175 SW 112th Ave.
Beaverton,  OR  97008
Applicant Contact BRADLEY A COHEN
Correspondent
Vidco, Inc.
6175 SW 112th Ave.
Beaverton,  OR  97008
Correspondent Contact BRADLEY A COHEN
Regulation Number870.2450
Classification Product Code
DXJ  
Date Received08/23/1993
Decision Date 08/18/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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