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FDA 510(k)

Endoscopic Video Image Processor (RP-IPD-V1000F)

K-Number: K243321 · 2025-02-07

Decision Date2025-02-07
Product CodeFET
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Endoscopic Video Image Processor (RP-IPD-V1000F) is a medical device manufactured by Guangzhou Red Pine Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2025-02-07 under approval number K243321. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Endoscopic Video Image Processor (RP-IPD-V1000F)?

Endoscopic Video Image Processor (RP-IPD-V1000F) is a medical device that received FDA 510(k) clearance on 2025-02-07. It is manufactured by Guangzhou Red Pine Medical Instrument Co., Ltd.. The 510(k) number is K243321.

When was Endoscopic Video Image Processor (RP-IPD-V1000F) approved by the FDA?

Endoscopic Video Image Processor (RP-IPD-V1000F) received FDA 510(k) clearance on 2025-02-07, under approval number K243321.

What company makes Endoscopic Video Image Processor (RP-IPD-V1000F)?

Endoscopic Video Image Processor (RP-IPD-V1000F) is manufactured by Guangzhou Red Pine Medical Instrument Co., Ltd..

What is the FDA product code for Endoscopic Video Image Processor (RP-IPD-V1000F)?

The FDA product code for Endoscopic Video Image Processor (RP-IPD-V1000F) is FET.

Related Clinical Trials

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Official Source

View on FDA Database →

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