Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K172346
Device Classification Name
System, Image Processing, Radiological
More FDA Info for this Device
510(K) Number
K172346
Device Name
System, Image Processing, Radiological
Applicant
EOS imaging
10 rue Mercoeur
Paris 75011 FR
Other 510(k) Applications for this Company
Contact
Mathias Breuil
Other 510(k) Applications for this Contact
Regulation Number
892.2050
More FDA Info for this Regulation Number
Classification Product Code
LLZ
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/03/2017
Decision Date
06/19/2018
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact