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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Full-Montage Standard Electroencephalograph
510(k) Number K802296
Device Name MINGOGRAF EEG10
Applicant
SIEMENS CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
SIEMENS CORP.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number882.1400
Classification Product Code
GWQ  
Date Received09/19/1980
Decision Date 10/03/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
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