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

INSTATRAK SYSTEM WITH MULTIPLE DATASET NAVIGATION, MODEL IT3500

K Number: K040050 · Decision Mar 24, 2004
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
1
Review Days
72

Basic Information

Device Name
INSTATRAK SYSTEM WITH MULTIPLE DATASET NAVIGATION, MODEL IT3500
K Number
K040050
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE MEDICAL SYSTEMS NAVIGATION AND VISUALIZATION IN
Date Received
January 12, 2004
Decision Date
March 24, 2004
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

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