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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name system, monitoring, perinatal
510(k) Number K771379
Device Name FETAL MONITORING SYS. MODEL FM3R
Applicant
SONICAID, INC.
803 N. Front St. Suite 3
mchenry,  IL  60050
Correspondent
SONICAID, INC.
803 N. Front St. Suite 3
mchenry,  IL  60050
Regulation Number884.2740
Classification Product Code
HGM  
Date Received07/26/1977
Decision Date 08/03/1977
Decision substantially equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
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