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. The listed applicant is Guangzhou Red Pine Medical Instrument Co., Ltd.. The 510(k) number is K243321.
When did Endoscopic Video Image Processor (RP-IPD-V1000F) receive FDA 510(k) clearance?
Endoscopic Video Image Processor (RP-IPD-V1000F) received FDA 510(k) clearance on 2025-02-07, under 510(k) number K243321.
Who is the listed applicant for Endoscopic Video Image Processor (RP-IPD-V1000F)?
The FDA 510(k) record lists Guangzhou Red Pine Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Guangzhou Red Pine 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.
Related Devices (Code: FET)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.