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OTRIEVA TAPERED OVUM ASPIRATION NEEDLE SINGLE LUMEN

K141365 Class II Special
Decision Date
2014-08-07
Sponsor / Applicant
William A. Cook Australia Pty. , Ltd.

Technical Specification

510(k) Submission ID K141365
Product Code MQE
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6100
Decision Date 2014-08-07
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OTRIEVA TAPERED OVUM ASPIRATION NEEDLE SINGLE LUMEN received FDA 510(k) clearance under submission number K141365, 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 2014-08-07.

Classification & Regulation

This clearance is catalogued under FDA product code MQE and 21 CFR 884.6100, within the Obstetrics/Gynecology review panel as a Class II device.