meddevicedb.com FDA Device Reference

Vitrification Solution Set and Warming Solution Set

K233846 Class II Traditional
Decision Date
2024-08-27
Sponsor / Applicant
Ecmpc, LLC

Technical Specification

510(k) Submission ID K233846
Product Code MQL
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6180
Decision Date 2024-08-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Vitrification Solution Set and Warming Solution Set received FDA 510(k) clearance under submission number K233846, sponsored by Ecmpc, LLC. 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 2024-08-27.

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.