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SYDNEY IVF EMBRYO BIOPSY MEDIUM

K152904 Class II Special
Decision Date
2015-12-03
Sponsor / Applicant
William A. Cook Australia Pty. , Ltd.

Technical Specification

510(k) Submission ID K152904
Product Code MQL
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6180
Decision Date 2015-12-03
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYDNEY IVF EMBRYO BIOPSY MEDIUM received FDA 510(k) clearance under submission number K152904, sponsored by William A. Cook Australia Pty. , Ltd.. 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 2015-12-03.

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.