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FDA 510(k) Application Details - K173517
Device Classification Name
System, X-Ray, Stationary
More FDA Info for this Device
510(K) Number
K173517
Device Name
System, X-Ray, Stationary
Applicant
SHIMADZU corporation
1 Nishinokyo-Kuwabaracho Nakagyo-ku
Kyoto 604-8511 JP
Other 510(k) Applications for this Company
Contact
Toshio Kadowaki
Other 510(k) Applications for this Contact
Regulation Number
892.1680
More FDA Info for this Regulation Number
Classification Product Code
KPR
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/14/2017
Decision Date
03/30/2018
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
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