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FDA 510(k)

Neorad Pacs (Neorad Pacs)

K-Number: K232641 · 2024-04-10

ApplicantEverrtech Software Pvt, Ltd.
Decision Date2024-04-10
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Neorad Pacs (Neorad Pacs) is a medical device manufactured by Everrtech Software Pvt, Ltd.. It received FDA 510(k) clearance on 2024-04-10 under approval number K232641. 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 Neorad Pacs (Neorad Pacs)?

Neorad Pacs (Neorad Pacs) is a medical device that received FDA 510(k) clearance on 2024-04-10. It is manufactured by Everrtech Software Pvt, Ltd.. The 510(k) number is K232641.

When was Neorad Pacs (Neorad Pacs) approved by the FDA?

Neorad Pacs (Neorad Pacs) received FDA 510(k) clearance on 2024-04-10, under approval number K232641.

What company makes Neorad Pacs (Neorad Pacs)?

Neorad Pacs (Neorad Pacs) is manufactured by Everrtech Software Pvt, Ltd..

What is the FDA product code for Neorad Pacs (Neorad Pacs)?

The FDA product code for Neorad Pacs (Neorad Pacs) is LLZ.

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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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