Cleared Traditional

K251986 - AUXILIARY WATER TUBE MAJ-855 (FDA 510(k) Clearance)

Sep 2025
Decision
91d
Days
Class 2
Risk

K251986 is an FDA 510(k) clearance for the AUXILIARY WATER TUBE MAJ-855. This device is classified as a Endoscopic Irrigation/suction System (Class II - Special Controls, product code OCX).

Submitted by Olympus Medical Systems Corporation (Hachioji-Shi, JP). The FDA issued a Cleared decision on September 26, 2025, 91 days after receiving the submission on June 27, 2025.

This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.1500. To Supply Sterile Water, Other Solutions And/or Suction To Endoscopes During Endoscopic Procedures..

Submission Details

510(k) Number K251986 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 27, 2025
Decision Date September 26, 2025
Days to Decision 91 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.