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FDA 510(k)

LiveMedica Enterprise PACS

K-Number: K253927 · 2026-02-06

ApplicantLive Medica, LLC
Decision Date2026-02-06
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LiveMedica Enterprise PACS is a medical device manufactured by Live Medica, LLC. It received FDA 510(k) clearance on 2026-02-06 under approval 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. It is manufactured by Live Medica, LLC. The 510(k) number is K253927.

When was LiveMedica Enterprise PACS approved by the FDA?

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

What company makes LiveMedica Enterprise PACS?

LiveMedica Enterprise PACS is manufactured by Live Medica, LLC.

What is the FDA product code for LiveMedica Enterprise PACS?

The FDA product code for LiveMedica Enterprise PACS is LLZ.

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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.

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