510(k) K151780

CAAS Workstation by Pie Medical Imaging BV — Product Code IZI

K151780 is an FDA 510(k) premarket notification submitted by Pie Medical Imaging BV for the device "CAAS Workstation". The FDA issued a decision of Substantially Equivalent on March 11, 2016. The device falls under product code IZI (System, X-Ray, Angiographic), a Class II device regulated under 21 CFR 892.1600. Pie Medical Imaging BV has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 11, 2016
Date Received
July 1, 2015
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, X-Ray, Angiographic
Device Class
Class II
Regulation Number
892.1600
Review Panel
RA
Submission Type