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

DISCOVERY MODEL CT590 RT AND OPTIMA MODEL CT580 CT SYSTEMS

K Number: K093581 · Decision Apr 19, 2011
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
795
Applicant Total
61
Review Days
517

Basic Information

Device Name
DISCOVERY MODEL CT590 RT AND OPTIMA MODEL CT580 CT SYSTEMS
K Number
K093581
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE MEDICAL SYSTEMS, LLC
Date Received
November 18, 2009
Decision Date
April 19, 2011
Product Code
JAK
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
JAK System, X-Ray, Tomography, Computed

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