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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name System, Nuclear Magnetic Resonance Imaging
510(k) Number K911667
Device Name HITACHI MRP-7000 MAGNETIC ROSONANCE DEVICE
Applicant
Hitachi Medical Systems America, Inc.
1963 Case Pkwy.
Twinsburg,  OH  44087
Applicant Contact ROBERT MCCARTHY
Correspondent
Hitachi Medical Systems America, Inc.
1963 Case Pkwy.
Twinsburg,  OH  44087
Correspondent Contact ROBERT MCCARTHY
Regulation Number892.1000
Classification Product Code
LNH  
Date Received04/12/1991
Decision Date 05/30/1991
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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