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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Electrocardiograph
510(k) Number K892835
Device Name E350 ELECTROCARDIOGRAPH
Applicant
Burdick Corp.
15 Plumb St.
Miltoon,  WI  53563
Applicant Contact FRANCIS I DOMINY
Correspondent
Burdick Corp.
15 Plumb St.
Miltoon,  WI  53563
Correspondent Contact FRANCIS I DOMINY
Regulation Number870.2340
Classification Product Code
DPS  
Date Received04/18/1989
Decision Date 06/01/1989
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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