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FDA 510(k)

Digital Video Processor

K-Number: K243117 · 2025-01-29

ApplicantHunan Vathin Medical Instrument Co., Ltd.
Decision Date2025-01-29
Product CodeFGB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Digital Video Processor is a medical device manufactured by Hunan Vathin Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2025-01-29 under approval number K243117. The device is classified under product code FGB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Digital Video Processor?

Digital Video Processor is a medical device that received FDA 510(k) clearance on 2025-01-29. It is manufactured by Hunan Vathin Medical Instrument Co., Ltd.. The 510(k) number is K243117.

When was Digital Video Processor approved by the FDA?

Digital Video Processor received FDA 510(k) clearance on 2025-01-29, under approval number K243117.

What company makes Digital Video Processor?

Digital Video Processor is manufactured by Hunan Vathin Medical Instrument Co., Ltd..

What is the FDA product code for Digital Video Processor?

The FDA product code for Digital Video Processor is FGB.

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Other Devices by Hunan Vathin Medical Instrument Co., Ltd.

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Related Devices (Code: FGB)

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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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