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FDA 510(k)

Relu Creator

K-Number: K233925 · 2024-06-13

ApplicantRelu BV
Decision Date2024-06-13
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Relu Creator is a medical device manufactured by Relu BV. It received FDA 510(k) clearance on 2024-06-13 under approval number K233925. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Relu Creator?

Relu Creator is a medical device that received FDA 510(k) clearance on 2024-06-13. It is manufactured by Relu BV. The 510(k) number is K233925.

When was Relu Creator approved by the FDA?

Relu Creator received FDA 510(k) clearance on 2024-06-13, under approval number K233925.

What company makes Relu Creator?

Relu Creator is manufactured by Relu BV.

What is the FDA product code for Relu Creator?

The FDA product code for Relu Creator is QIH.

Other Devices by Relu BV

K252708Relu Cloud

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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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