Cleared Traditional

GYN-Pump PH304

K173489 · W.O.M. World of Medicine GmbH · Obstetrics & Gynecology
Mar 2018
Decision
135d
Days
Class 2
Risk

About This 510(k) Submission

K173489 is an FDA 510(k) clearance for the GYN-Pump PH304, a Insufflator, Hysteroscopic (Class II — Special Controls, product code HIG), submitted by W.O.M. World of Medicine GmbH (Berlin, DE). The FDA issued a Cleared decision on March 28, 2018, 135 days after receiving the submission on November 13, 2017. This device falls under the Obstetrics & Gynecology review panel. Regulated under 21 CFR 884.1700.

Submission Details

510(k) Number K173489 FDA.gov
FDA Decision Cleared SESE
Date Received November 13, 2017
Decision Date March 28, 2018
Days to Decision 135 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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