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

RADIOLOGICAL IMAGE PROCESSING SYSTEM

K Number: K102078 · Decision Aug 10, 2011
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
22
Review Days
380

Basic Information

Device Name
RADIOLOGICAL IMAGE PROCESSING SYSTEM
K Number
K102078
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
VATECH CO., LTD.
Date Received
July 26, 2010
Decision Date
August 10, 2011
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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