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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stimulator, Muscle, Diagnostic
510(k) Number K780632
Device Name MAXICEPTOR
Applicant
Med General
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Med General
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number890.1850
Classification Product Code
ISB  
Date Received04/17/1978
Decision Date 08/14/1978
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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