FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

VISAGE PACS/CS, RELEASE VERSION 5.0

K Number: K072205 · Decision Aug 29, 2007
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
2
Review Days
21

Basic Information

Device Name
VISAGE PACS/CS, RELEASE VERSION 5.0
K Number
K072205
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MERCURY COMPUTER SYSTEMS, INC
Date Received
August 8, 2007
Decision Date
August 29, 2007
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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K Number Device Name
K062490 VISAGE PACS/CS, RELEASE VERSION 4.1