Cleared Traditional

K222695 - troCarWash? System
(FDA 510(k) Clearance)

K222695 · Biotex, Inc. · General & Plastic Surgery
Feb 2023
Decision
164d
Days
Class 2
Risk

K222695 is an FDA 510(k) clearance for the troCarWash? System. This device is classified as a Endoscopic Irrigation/suction System (Class II — Special Controls, product code OCX).

Submitted by Biotex, Inc. (Houston, US). The FDA issued a Cleared decision on February 17, 2023, 164 days after receiving the submission on September 6, 2022.

This device falls under the General & Plastic Surgery 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 K222695 FDA.gov
FDA Decision Cleared SESE
Date Received September 06, 2022
Decision Date February 17, 2023
Days to Decision 164 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
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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