meddevicedb.com FDA Device Reference

SAGE 1-Step GM-CSF with HSA, SAGE 1-Step GM-CSF with SPS

K172197 Class II Traditional
Decision Date
2017-10-13
Sponsor / Applicant
Origio A/S

Technical Specification

510(k) Submission ID K172197
Product Code MQL
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6180
Decision Date 2017-10-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SAGE 1-Step GM-CSF with HSA, SAGE 1-Step GM-CSF with SPS received FDA 510(k) clearance under submission number K172197, sponsored by Origio A/S. 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 2017-10-13.

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.