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Guardia™ Access Nano and Soft-Trans Embryo Transfer Catheter Sets, Soft-Trans Embryo Transfer Catheter, Soft-Trans Guide Catheter

K172051 Class II Traditional
Decision Date
2018-01-10
Sponsor / Applicant
Cook Incorporated

Technical Specification

510(k) Submission ID K172051
Product Code MQF
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6110
Decision Date 2018-01-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Guardia™ Access Nano and Soft-Trans Embryo Transfer Catheter Sets, Soft-Trans Embryo Transfer Catheter, Soft-Trans Guide Catheter received FDA 510(k) clearance under submission number K172051, 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 2018-01-10.

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.