meddevicedb.com FDA Device Reference

Pivet and Soft-Pass Embryo Transfer Catheter Sets

K173103 Class II Traditional
Decision Date
2018-04-13
Sponsor / Applicant
Cook Incorporated

Technical Specification

510(k) Submission ID K173103
Product Code MQF
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6110
Decision Date 2018-04-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Pivet and Soft-Pass Embryo Transfer Catheter Sets received FDA 510(k) clearance under submission number K173103, sponsored by Cook Incorporated. 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 2018-04-13.

Classification & Regulation

This clearance is catalogued under FDA product code MQF and 21 CFR 884.6110, within the Obstetrics/Gynecology review panel as a Class II device.