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FDA 510(k)

Digital Video Processor

K-Number: K243117 · 2025-01-29

Decision Date2025-01-29
Product CodeFGB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Digital Video Processor is the device name listed in this FDA 510(k) record. The listed applicant is Hunan Vathin Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2025-01-29 under 510(k) 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. The listed applicant is Hunan Vathin Medical Instrument Co., Ltd.. The 510(k) number is K243117.

When did Digital Video Processor receive FDA 510(k) clearance?

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

Who is the listed applicant for Digital Video Processor?

The FDA 510(k) record lists Hunan Vathin Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Digital Video Processor?

The FDA product code for Digital Video Processor is FGB.

Other records listing Hunan Vathin Medical Instrument Co., Ltd. as applicant

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.

View all 17 devices →

Related Devices (Code: FGB)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.