510(k) K212376

Caas Qardia by Pie Medical Imaging BV — Product Code LLZ

K212376 is an FDA 510(k) premarket notification submitted by Pie Medical Imaging BV for the device "Caas Qardia". The FDA issued a decision of Substantially Equivalent on May 16, 2022. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Pie Medical Imaging BV has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 16, 2022
Date Received
July 30, 2021
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Image Processing, Radiological
Device Class
Class II
Regulation Number
892.2050
Review Panel
RA
Submission Type