FDA 510(k)

LiveMedica Enterprise PACS

K-Number: K253927 · 2026-02-06

Decision Date2026-02-06

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

LiveMedica Enterprise PACS is the device name listed in this FDA 510(k) record. The listed applicant is Live Medica, LLC. It received FDA 510(k) clearance on 2026-02-06 under 510(k) number K253927. 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 LiveMedica Enterprise PACS?

LiveMedica Enterprise PACS is a medical device that received FDA 510(k) clearance on 2026-02-06. The listed applicant is Live Medica, LLC. The 510(k) number is K253927.

When did LiveMedica Enterprise PACS receive FDA 510(k) clearance?

LiveMedica Enterprise PACS received FDA 510(k) clearance on 2026-02-06, under 510(k) number K253927.

Who is the listed applicant for LiveMedica Enterprise PACS?

The FDA 510(k) record lists Live Medica, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LiveMedica Enterprise PACS?

The FDA product code for LiveMedica Enterprise 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.

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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.