meddevicedb.com FDA Device Reference

Sydney IVF Hyaluronidase

K151367 Class II Traditional
Decision Date
2016-01-27
Sponsor / Applicant
William A. Cook Australia Pty. , Ltd.

Technical Specification

510(k) Submission ID K151367
Product Code MQL
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6180
Decision Date 2016-01-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Sydney IVF Hyaluronidase received FDA 510(k) clearance under submission number K151367, sponsored by William A. Cook Australia Pty. , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2016-01-27.

Classification & Regulation

This clearance is catalogued under FDA product code MQL and 21 CFR 884.6180, within the Obstetrics/Gynecology review panel as a Class II device.