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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 K955931
Device Name MODEL IM77 INTRAPARTUM FETAL MONITOR (MODIFICATION)
Applicant
ADVANCED MEDICAL SYSTEMS, INC.
925 SHERMAN AVE.
HAMDEN,  CT  06514
Applicant Contact ANTHONY CALDERONI
Correspondent
ADVANCED MEDICAL SYSTEMS, INC.
925 SHERMAN AVE.
HAMDEN,  CT  06514
Correspondent Contact ANTHONY CALDERONI
Regulation Number884.2740
Classification Product Code
HGM  
Subsequent Product Code
DQA  
Date Received12/15/1995
Decision Date 08/14/1996
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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