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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Monitor, Heart Rate, Fetal, Ultrasonic
510(k) Number K930714
Device Name SONICAID MODEL TEAM FECG IUP
Applicant
Oxford Instruments, Plc.
11526 53rd.St. N.
Clearwater,  FL  34620
Applicant Contact MICHAEL J SMITH
Correspondent
Oxford Instruments, Plc.
11526 53rd.St. N.
Clearwater,  FL  34620
Correspondent Contact MICHAEL J SMITH
Regulation Number884.2660
Classification Product Code
HEL  
Date Received02/11/1993
Decision Date 08/24/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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