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

VITREA2 VERSION 3.8 MEDICAL IMAGE PROCESSING SOFTWARE

K Number: K052632 · Decision Dec 15, 2005
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
30
Review Days
80

Basic Information

Device Name
VITREA2 VERSION 3.8 MEDICAL IMAGE PROCESSING SOFTWARE
K Number
K052632
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
VITAL IMAGES, INC.
Date Received
September 26, 2005
Decision Date
December 15, 2005
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

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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