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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Kuros Biosciences B.V. It received FDA 510(k) clearance on 2024-01-19 under 510(k) 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. The listed applicant is Kuros Biosciences B.V. The 510(k) number is K232347.

When did MagnetOs Granules receive FDA 510(k) clearance?

MagnetOs Granules received FDA 510(k) clearance on 2024-01-19, under 510(k) number K232347.

Who is the listed applicant for MagnetOs Granules?

The FDA 510(k) record lists Kuros Biosciences B.V as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MagnetOs Granules?

The FDA product code for MagnetOs Granules is MQV.

Other records listing Kuros Biosciences B.V as applicant

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Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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