FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

FC 700 FETAL MONITOR

K Number: K043597 · Decision Dec 16, 2005
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
213
Applicant Total
11
Review Days
352

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Basic Information

Device Name
FC 700 FETAL MONITOR
K Number
K043597
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.2740
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bionet Co., Ltd.
Date Received
December 29, 2004
Decision Date
December 16, 2005
Product Code
HGM
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HGM System, Monitoring, Perinatal

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K130322 SPM-300
K113306 CARDIO 7
K102767 CARDIO XP
K090895 EKG-PLUS II SOFTWARE
K082008 BIONET BM3PLUS PATIENT MONITOR
K043598 FC 1400 FETAL MONITOR
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