Cleared Traditional

Endoscopy Irrigation Tubing

K230773 · Zhejiang Chuangxiang Medical Technology Co., Ltd. · Gastroenterology & Urology
Nov 2023
Decision
245d
Days
Class 2
Risk

About This 510(k) Submission

K230773 is an FDA 510(k) clearance for the Endoscopy Irrigation Tubing, a Endoscopic Irrigation/suction System (Class II — Special Controls, product code OCX), submitted by Zhejiang Chuangxiang Medical Technology Co., Ltd. (Hangzhou, CN). The FDA issued a Cleared decision on November 21, 2023, 245 days after receiving the submission on March 21, 2023. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.

Submission Details

510(k) Number K230773 FDA.gov
FDA Decision Cleared SESE
Date Received March 21, 2023
Decision Date November 21, 2023
Days to Decision 245 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code OCX — Endoscopic Irrigation/suction System
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.1500
Definition To Supply Sterile Water, Other Solutions And/or Suction To Endoscopes During Endoscopic Procedures.

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