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FDA 510(k)

Neorad Pacs (Neorad Pacs)

K-Number: K232641 · 2024-04-10

Decision Date2024-04-10
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Neorad Pacs (Neorad Pacs) is the device name listed in this FDA 510(k) record. The listed applicant is Everrtech Software Pvt, Ltd.. It received FDA 510(k) clearance on 2024-04-10 under 510(k) 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. The listed applicant is Everrtech Software Pvt, Ltd.. The 510(k) number is K232641.

When did Neorad Pacs (Neorad Pacs) receive FDA 510(k) clearance?

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

Who is the listed applicant for Neorad Pacs (Neorad Pacs)?

The FDA 510(k) record lists Everrtech Software Pvt, Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

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

Official Source

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