Cleared Traditional

Disposable Endoscopy Adapter Set

K220210 · Yangzhou Fartley Medical Instrument Technology Co., Ltd. · Gastroenterology & Urology
Jun 2022
Decision
142d
Days
Class 2
Risk

About This 510(k) Submission

K220210 is an FDA 510(k) clearance for the Disposable Endoscopy Adapter Set, a Endoscope Channel Accessory (Class II — Special Controls, product code ODC), submitted by Yangzhou Fartley Medical Instrument Technology Co., Ltd. (Yangzhou, CN). The FDA issued a Cleared decision on June 17, 2022, 142 days after receiving the submission on January 26, 2022. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.

Submission Details

510(k) Number K220210 FDA.gov
FDA Decision Cleared SESE
Date Received January 26, 2022
Decision Date June 17, 2022
Days to Decision 142 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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