SterEOS Workstation

System, Image Processing, Radiological

EOS Imaging

The following data is part of a premarket notification filed by Eos Imaging with the FDA for Stereos Workstation.

Pre-market Notification Details

Device IDK172346
510k NumberK172346
Device Name:SterEOS Workstation
ClassificationSystem, Image Processing, Radiological
Applicant EOS Imaging 10 Rue Mercoeur Paris,  FR 75011
ContactMathias Breuil
CorrespondentMathias Breuil
EOS Imaging 10 Rue Mercoeur Paris,  FR 75011
Product CodeLLZ  
CFR Regulation Number892.2050 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2017-08-03
Decision Date2018-06-19
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
03663999000153 K172346 000

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