meddevicedb.com FDA Device Reference

HYSTEROSCOPY PUMP HM6

K123732 Class II Special
Decision Date
2013-04-04
Sponsor / Applicant
W.O.M. World of Medicine AG

Technical Specification

510(k) Submission ID K123732
Product Code HIG
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.1700
Decision Date 2013-04-04
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HYSTEROSCOPY PUMP HM6 received FDA 510(k) clearance under submission number K123732, sponsored by W.O.M. World of Medicine AG. The device was reviewed via the Special premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2013-04-04.

Classification & Regulation

This clearance is catalogued under FDA product code HIG and 21 CFR 884.1700, within the Obstetrics/Gynecology review panel as a Class II device.