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

GE INNOVA SOLID STATE XRAY IMAGER FLUROSOPIC X RAY SYSTEM

K Number: K113034 · Decision Dec 13, 2011
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
195
Applicant Total
119
Review Days
63

Basic Information

Device Name
GE INNOVA SOLID STATE XRAY IMAGER FLUROSOPIC X RAY SYSTEM
K Number
K113034
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1600
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE HEALTHCARE
Date Received
October 11, 2011
Decision Date
December 13, 2011
Product Code
IZI
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
IZI System, X-Ray, Angiographic

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