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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 K813457
Device Name FETASCAN 2000,2000A OBSTETRICAL DATA
Applicant
CRANBURY MEDICAL LABS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
CRANBURY MEDICAL LABS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number884.2740
Classification Product Code
HGM  
Date Received12/10/1981
Decision Date 02/12/1982
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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