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FDA 510(k)

ZeTTA PACS

K-Number: K241694 · 2025-01-31

ApplicantTae Young Soft Co., Ltd.
Decision Date2025-01-31
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ZeTTA PACS is a medical device manufactured by Tae Young Soft Co., Ltd.. It received FDA 510(k) clearance on 2025-01-31 under approval number K241694. 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 ZeTTA PACS?

ZeTTA PACS is a medical device that received FDA 510(k) clearance on 2025-01-31. It is manufactured by Tae Young Soft Co., Ltd.. The 510(k) number is K241694.

When was ZeTTA PACS approved by the FDA?

ZeTTA PACS received FDA 510(k) clearance on 2025-01-31, under approval number K241694.

What company makes ZeTTA PACS?

ZeTTA PACS is manufactured by Tae Young Soft Co., Ltd..

What is the FDA product code for ZeTTA PACS?

The FDA product code for ZeTTA 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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