MagnetOs Granules
K-Number: K232347 · 2024-01-19
ApplicantKuros Biosciences B.V
Decision Date2024-01-19
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
MagnetOs Granules is a medical device manufactured by Kuros Biosciences B.V. It received FDA 510(k) clearance on 2024-01-19 under approval number K232347. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MagnetOs Granules?
MagnetOs Granules is a medical device that received FDA 510(k) clearance on 2024-01-19. It is manufactured by Kuros Biosciences B.V. The 510(k) number is K232347.
When was MagnetOs Granules approved by the FDA?
MagnetOs Granules received FDA 510(k) clearance on 2024-01-19, under approval number K232347.
What company makes MagnetOs Granules?
MagnetOs Granules is manufactured by Kuros Biosciences B.V.
What is the FDA product code for MagnetOs Granules?
The FDA product code for MagnetOs Granules is MQV.
Related Clinical Trials
Other Devices by Kuros Biosciences B.V
Related Devices (Code: MQV)
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.