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FDA 510(k) Application Details - K143695
Device Classification Name
System, Monitoring, Perinatal
More FDA Info for this Device
510(K) Number
K143695
Device Name
System, Monitoring, Perinatal
Applicant
EDAN INSTRUMENTS INC
3/F - B, NANSHAN MEDICAL EQUIPMENTS PARK
NANHAI RD 1019#
SHENZHEN 518067 CN
Other 510(k) Applications for this Company
Contact
QUEENA CHEN
Other 510(k) Applications for this Contact
Regulation Number
884.2740
More FDA Info for this Regulation Number
Classification Product Code
HGM
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/24/2014
Decision Date
03/30/2015
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OB - Obstetrics/Gynecology
Review Advisory Committee
OB - Obstetrics/Gynecology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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