Cleared Traditional

HYS-SURGIMAT

K934866 · W.O.M. World of Medicine GmbH · Obstetrics & Gynecology
Oct 1995
Decision
738d
Days
Class 2
Risk

About This 510(k) Submission

K934866 is an FDA 510(k) clearance for the HYS-SURGIMAT, a Insufflator, Hysteroscopic (Class II — Special Controls, product code HIG), submitted by W.O.M. World of Medicine GmbH (Washington, US). The FDA issued a Cleared decision on October 20, 1995, 738 days after receiving the submission on October 12, 1993. This device falls under the Obstetrics & Gynecology review panel. Regulated under 21 CFR 884.1700.

Submission Details

510(k) Number K934866 FDA.gov
FDA Decision Cleared SESE
Date Received October 12, 1993
Decision Date October 20, 1995
Days to Decision 738 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

Similar Devices — HIG Insufflator, Hysteroscopic

All 54
Fluent Pro Fluid Management System (FLT-200); Fluent Pro Fluid Management System Disposable Procedure Kit (6-pack) (FLT-212); Fluent Pro Fluid Management System Disposable Procedure Kit (1-pack) (FLT-212S); Fluent Pro Fluid Management System Tissue Trap Multipack (10-pack) (FLT-210); Fluent Pro Fluid Management System Waste Bag Multipack (5-pack) (FLT-205)
K240886 · Hologic, Inc. · Jul 2024
X-FLO Fluid Management System
K210628 · Thermedx, LLC · Nov 2021
Endomat Select, IBS Shaver Software, License
K201355 · Karl Storz SE & CO. KG · Jul 2020
Endomat Select
K180735 · Karl Storz SE & CO. KG · Oct 2018
Fluent Fluid Management System
K180825 · Hologic, Inc. · Aug 2018
GYN-Pump PH304
K173489 · W.O.M. World of Medicine GmbH · Mar 2018