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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 K992886
Device Name POWERVIEW ULTRASOUND WORKSTATION, UIDM-400A
Original Applicant
TOSHIBA AMERICA MEDICAL SYSTEMS, INC.
2441 michelle dr.
p.o. box 2068
tustin,  CA  92781 -2068
Original Contact paul biggins
Regulation Number892.2050
Classification Product Code
LLZ  
Date Received08/26/1999
Decision Date 11/09/1999
Decision substantially equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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