K243321
- 510(k) number
- K243321
- Device name
- Endoscopic Video Image Processor (RP-IPD-V1000F)
- Applicant
- Guangzhou Red Pine Medical Instrument Co., Ltd. CN
- Product code
- FET — Endoscopic Video Imaging System/Component, Gastroent
- Decision date
- 2025-02-07
- Date received
- 2024-10-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
510(k) Summary (official FDA PDF): K243321.pdf
Official FDA record: K243321
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.