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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Permanent Pacemaker Electrode
510(k) Number K920822
Device Name CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE
Applicant
Siemens-Pacesetter, Inc.
15900 Valley View Ct.
P.O. Box 9221
Sylmar,  CA  91392
Applicant Contact GLENN THOMPSON
Correspondent
Siemens-Pacesetter, Inc.
15900 Valley View Ct.
P.O. Box 9221
Sylmar,  CA  91392
Correspondent Contact GLENN THOMPSON
Regulation Number870.3680
Classification Product Code
DTB  
Date Received02/24/1992
Decision Date 01/22/1993
Decision SE - Postmarket Surveillance Required (SESP)
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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