Cleared Traditional

Disposable Distal Attachment D-201 Series

K250296 · Olympus Medical Systems Corp. · Gastroenterology & Urology
May 2025
Decision
90d
Days
Class 2
Risk

About This 510(k) Submission

K250296 is an FDA 510(k) clearance for the Disposable Distal Attachment D-201 Series, a Gastroscope And Accessories, Flexible/rigid (Class II — Special Controls, product code FDS), submitted by Olympus Medical Systems Corp. (Hachiochi-Shi, JP). The FDA issued a Cleared decision on May 1, 2025, 90 days after receiving the submission on January 31, 2025. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.

Submission Details

510(k) Number K250296 FDA.gov
FDA Decision Cleared SESE
Date Received January 31, 2025
Decision Date May 01, 2025
Days to Decision 90 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code FDS — Gastroscope And Accessories, Flexible/rigid
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.1500
Definition To Examine Or Perform Procedures In The Stomach. For Reusable, Flexible Endoscopes In This Product Code, Validated Reprocessing Instructions And Reprocessing Validation Data Must Be Included In A 510(k) Submission (82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).

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