# K241500: Endoscopic Video Image Processor (RP-IPD-V2000EF); Single-Use Video Flexible Cysto-Nephroscope (RP-U-C01F, RP-U-C01FS)

- Pathway: 510(k) (Traditional)
- Applicant: Guangzhou Red Pine Medical Instrument Co., Ltd.
- Decided: Jul 12, 2024 after 45 days
- Product code: FAJ (Cystoscope And Accessories, Flexible/Rigid)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K931154 (1993). 19 ancestors in all.
2 later devices descend from it; 2 cite it directly.
1 of 22 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133538: Visera Cysto-Nephro Videoscope Olympus Cyf Type V2, Visera Cysto-Nephro Videoscope Olympus Cyf Type VA2, Visera Cysto-NE, Olympus Corporation of the Americas (2014) Summary page 5.

## Most influential descendants
- K252176: Single-Use Video Flexible Cysto-Nephroscope (RP-U-C01F, RP-U-C01FS) (2025), 0 descendants of its own
- K243321: Endoscopic Video Image Processor (RP-IPD-V1000F) (2025), 0 descendants of its own

## Indications for use
Endoscopic Video Image Processor This device is used in conjunction with the video endoscopes produced by our company to process the images collected by the video endoscopes and send them to the display, and provide power for the endoscope. Single-Use Video Flexible Cysto-Nephroscope This product shall be used in conjunction with the Endoscopic Video Image Processor and other peripheral equipment for observation, diagnosis, photography and treatment within the bladder, urethra, and kidney. The device is suitable for professional healthcare facility environments such as hospitals and clinics. This product shall not be used for other purposes.

Source page: https://510kreport.com/device/K241500
Methodology: https://510kreport.com/methodology