FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

EOS System

K Number: K142773 · Decision Jan 22, 2015
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
15
Review Days
119

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Basic Information

Device Name
EOS System
K Number
K142773
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Eos Imaging
Date Received
September 25, 2014
Decision Date
January 22, 2015
Product Code
KPR
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
KPR System, X-Ray, Stationary

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KPR), ordered by most recent decision date.

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Other Clearances by Eos Imaging

K Number Device Name
K251078 AutoDensity
K251747 VEA Align; spineEOS
K233920 EOSedge
K240582 VEA Align; spineEOS
K231917 VEA Align
K232086 spineEOS
K202394 EOSedge
K192079 EOSedge
K172346 sterEOS Workstation
K152788 EOS System
Search all 15 clearances from Eos Imaging →