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

DOPPLEX CENTRALE

K Number: K060230 · Decision Mar 23, 2006
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
213
Applicant Total
8
Review Days
52

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Basic Information

Device Name
DOPPLEX CENTRALE
K Number
K060230
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 , Ltd.
Date Received
January 30, 2006
Decision Date
March 23, 2006
Product Code
HGM
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
Y

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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