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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Computer, Diagnostic, Pre-Programmed, Single-Function
510(k) Number K842706
Device Name SCATAID
Applicant
Sc Applied Technology, Inc.
1100 Ring Bldg.
1200 18th. St.
Washington,  DC  20036 -
Applicant Contact CLIFTON E MCCANN
Correspondent
Sc Applied Technology, Inc.
1100 Ring Bldg.
1200 18th. St.
Washington,  DC  20036 -
Correspondent Contact CLIFTON E MCCANN
Regulation Number870.1435
Classification Product Code
DXG  
Date Received07/12/1984
Decision Date 11/27/1984
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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