Cleared Traditional

X-FLO Fluid Management System

K210628 · Thermedx, LLC · Obstetrics & Gynecology
Nov 2021
Decision
247d
Days
Class 2
Risk

About This 510(k) Submission

K210628 is an FDA 510(k) clearance for the X-FLO Fluid Management System, a Insufflator, Hysteroscopic (Class II — Special Controls, product code HIG), submitted by Thermedx, LLC (Solon, US). The FDA issued a Cleared decision on November 4, 2021, 247 days after receiving the submission on March 2, 2021. This device falls under the Obstetrics & Gynecology review panel. Regulated under 21 CFR 884.1700.

Submission Details

510(k) Number K210628 FDA.gov
FDA Decision Cleared SESE
Date Received March 02, 2021
Decision Date November 04, 2021
Days to Decision 247 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF

Device Classification

Product Code HIG — Insufflator, Hysteroscopic
Device Class Class II — Special Controls
CFR Regulation 21 CFR 884.1700

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