Endoscopic Video Image Processor (RP-IPD-V1000F)— 510(k) K243321
Substantially EquivalentGuangzhou Red Pine Medical Instrument Co., Ltd.
FDA 510(k) clearance K243321 for Endoscopic Video Image Processor (RP-IPD-V1000F), Substantially Equivalent on 2025-02-07. Applicant: Guangzhou Red Pine Medical Instrument Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Guangzhou Red Pine Medical Instrument Co., Ltd.
- Product code
- Code FET
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Guangzhou, CN
Recent devices under product code FET
view allMore clearances from Guangzhou Red Pine Medical Instrument Co., Ltd.
view all- K251951 — Single-Use Video Flexible Ureterorenoscope (RP-U-C03R9, RP-U-C03R3, RP-U-C03S9, RP-U-C03S3) +2 more
- K252176 — Single-Use Video Flexible Cysto-Nephroscope (RP-U-C01F, RP-U-C01FS)
- K241987 — Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101)
- K241500 — Endoscopic Video Image Processor (RP-IPD-V2000EF); Single-Use Video Flexible Cysto-Nephroscope (RP-U-C01F, RP-U-C01FS)
- K240663 — Single-Use Video Flexible Cystoscope (RP-U-C0201/RP-U-C0201S)
Adverse events under product code FET
product code FET- Injury
- 313
- Malfunction
- 54,276
- Total
- 54,589
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.