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

UNISIGHT SYSTEM WITH UNIGATE

K Number: K023394 · Decision Jan 7, 2003
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
3
Review Days
90

Basic Information

Device Name
UNISIGHT SYSTEM WITH UNIGATE
K Number
K023394
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ELECTRONIC BUSINESS MACHINE CO., LTD. (EBM)
Date Received
October 9, 2002
Decision Date
January 7, 2003
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
K071166 UNIWEB, VERSION 5.0
K062743 UNISIGHT MAMMOGRAPHY VIEWER, MODEL 4.0