Cleared Traditional

Disposable Endoscope Valves Kit

K222499 · Shanghai SeeGen Photoelectric Technology Co., Ltd. · Gastroenterology & Urology
Nov 2023
Decision
461d
Days
Class 2
Risk

About This 510(k) Submission

K222499 is an FDA 510(k) clearance for the Disposable Endoscope Valves Kit, a Endoscope Channel Accessory (Class II — Special Controls, product code ODC), submitted by Shanghai SeeGen Photoelectric Technology Co., Ltd. (Shanghai, CN). The FDA issued a Cleared decision on November 22, 2023, 461 days after receiving the submission on August 18, 2022. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.

Submission Details

510(k) Number K222499 FDA.gov
FDA Decision Cleared SESE
Date Received August 18, 2022
Decision Date November 22, 2023
Days to Decision 461 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code ODC — Endoscope Channel Accessory
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.1500
Definition To Give The Endoscope Channel Additional Or Improved Functionality.

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