Endoscopic Video Image Processor (RP-IPD-V1000F)
K-Number: K243321 · 2025-02-07
Device Summary
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
Other Devices by Guangzhou Red Pine Medical Instrument Co., Ltd.
Related Devices (Code: FET)
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.