CAAS MR Solutions
K-Number: K232007 · 2024-02-01
ApplicantPie Medical Imaging BV
Decision Date2024-02-01
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
CAAS MR Solutions is a medical device manufactured by Pie Medical Imaging BV. It received FDA 510(k) clearance on 2024-02-01 under approval number K232007. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the CAAS MR Solutions?
CAAS MR Solutions is a medical device that received FDA 510(k) clearance on 2024-02-01. It is manufactured by Pie Medical Imaging BV. The 510(k) number is K232007.
When was CAAS MR Solutions approved by the FDA?
CAAS MR Solutions received FDA 510(k) clearance on 2024-02-01, under approval number K232007.
What company makes CAAS MR Solutions?
CAAS MR Solutions is manufactured by Pie Medical Imaging BV.
What is the FDA product code for CAAS MR Solutions?
The FDA product code for CAAS MR Solutions is LLZ.
Other Devices by Pie Medical Imaging BV
Related Devices (Code: LLZ)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.