FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

COR ANALYZER

K Number: K110071 · Decision Jan 31, 2011
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
3
Review Days
21

Basic Information

Device Name
COR ANALYZER
K Number
K110071
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
RCADIA MEDICAL IMAGING LTD.
Date Received
January 10, 2011
Decision Date
January 31, 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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K Number Device Name
K072242 COR ANALYZER II, MODEL V1.7
K063548 COR ANALYZER 1, VERSION 1.4