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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Monitor, Ultrasonic, Fetal
510(k) Number K800859
Device Name FETAL HEART DETECTOR #D206
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 Number884.2660
Classification Product Code
KNG  
Date Received04/15/1980
Decision Date 05/14/1980
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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