FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

GE LOGIQ I, LOGIQ E AND VIVID E

K Number: K113690 · Decision Dec 29, 2011
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
1117
Applicant Total
119
Review Days
14

Basic Information

Device Name
GE LOGIQ I, LOGIQ E AND VIVID E
K Number
K113690
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1550
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE HEALTHCARE
Date Received
December 15, 2011
Decision Date
December 29, 2011
Product Code
IYN
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
IYN System, Imaging, Pulsed Doppler, Ultrasonic

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