510(k) K152244

RADspeed Pro by Shimadzu Corporation — Product Code KPR

K152244 is an FDA 510(k) premarket notification submitted by Shimadzu Corporation for the device "RADspeed Pro". The FDA issued a decision of Substantially Equivalent on June 20, 2016. The device falls under product code KPR (System, X-Ray, Stationary), a Class II device regulated under 21 CFR 892.1680. Shimadzu Corporation has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 20, 2016
Date Received
August 10, 2015
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, X-Ray, Stationary
Device Class
Class II
Regulation Number
892.1680
Review Panel
RA
Submission Type