Relu Creator
K-Number: K233925 · 2024-06-13
Device Summary
Frequently Asked Questions
What is the Relu Creator?
Relu Creator is a medical device that received FDA 510(k) clearance on 2024-06-13. The listed applicant is Relu BV. The 510(k) number is K233925.
When did Relu Creator receive FDA 510(k) clearance?
Relu Creator received FDA 510(k) clearance on 2024-06-13, under 510(k) number K233925.
Who is the listed applicant for Relu Creator?
The FDA 510(k) record lists Relu BV as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Relu Creator?
The FDA product code for Relu Creator is QIH.
Other records listing Relu BV as applicant
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.
Related Devices (Code: QIH)
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.
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.