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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 K790386
Device Name LEAD MODELS MUM 1260, MUM 1290
Applicant
Ela Medical, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Ela Medical, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number870.3680
Classification Product Code
DTB  
Date Received02/26/1979
Decision Date 04/03/1979
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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