meddevicedb.com FDA Device Reference

Endoscopic Video Image Processor, Single-Use Video Hysteroscope

K232003 Class II Traditional
Decision Date
2024-02-12
Sponsor / Applicant
Guangzhou Red Pine Medical Instrument Co., Ltd.

Technical Specification

510(k) Submission ID K232003
Product Code HIH
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.1690
Decision Date 2024-02-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Endoscopic Video Image Processor, Single-Use Video Hysteroscope received FDA 510(k) clearance under submission number K232003, sponsored by Guangzhou Red Pine Medical Instrument Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2024-02-12.

Classification & Regulation

This clearance is catalogued under FDA product code HIH and 21 CFR 884.1690, within the Obstetrics/Gynecology review panel as a Class II device.