FDA 510(k)

OpenRad Cloud

K-Number: K240839 · 2024-04-24

Decision Date2024-04-24

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

OpenRad Cloud is the device name listed in this FDA 510(k) record. The listed applicant is Openrad Services Uk, Ltd.. It received FDA 510(k) clearance on 2024-04-24 under 510(k) number K240839. 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 OpenRad Cloud?

OpenRad Cloud is a medical device that received FDA 510(k) clearance on 2024-04-24. The listed applicant is Openrad Services Uk, Ltd.. The 510(k) number is K240839.

When did OpenRad Cloud receive FDA 510(k) clearance?

OpenRad Cloud received FDA 510(k) clearance on 2024-04-24, under 510(k) number K240839.

Who is the listed applicant for OpenRad Cloud?

The FDA 510(k) record lists Openrad Services Uk, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OpenRad Cloud?

The FDA product code for OpenRad Cloud is LLZ.

Related Devices (Code: LLZ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.