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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K837107
Device Name SOMATOM DRI X-RAY CT SCANNER
Applicant
Siemens Medical Solutions USA, Inc.
22010 SE 51st St.
Issaquah,  WA  98027
Correspondent
Siemens Medical Solutions USA, Inc.
22010 SE 51st St.
Issaquah,  WA  98027
Date Received01/31/1983
Decision Date 03/09/1983
Decision Substantially Equivalent (SESE)
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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