FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

SONICAID FREEDOM WIRELESS FETAL MONITORING SYSTEM

K Number: K132650 · Decision Feb 7, 2014
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
213
Applicant Total
3
Review Days
165

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Basic Information

Device Name
SONICAID FREEDOM WIRELESS FETAL MONITORING SYSTEM
K Number
K132650
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.2740
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Huntleigh Healthcare Limited
Date Received
August 26, 2013
Decision Date
February 7, 2014
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HGM), ordered by most recent decision date.

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Other Clearances by Huntleigh Healthcare Limited

K Number Device Name
K201425 Disposable Intraoperative Probe (DIOP8)
K200975 Sonicaid Team3 Antepartum, Sonicaid Team3 Intrapartum