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

GE VIVID E9 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM

K Number: K101149 · Decision Oct 13, 2010
Classifications
1
FEI Numbers
345
Registration Numbers
346
Same Product Code
883
Applicant Total
10
Review Days
173

Basic Information

Device Name
GE VIVID E9 DIAGNOSTIC ULTRASOUND IMAGING SYSTEM
K Number
K101149
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE VINGMED ULTRASOUND AS
Date Received
April 23, 2010
Decision Date
October 13, 2010
Product Code
IYO
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
IYO System, Imaging, Pulsed Echo, Ultrasonic

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