meddevicedb.com FDA Device Reference

MEDIA FOR GAMETE PREPARATION AND EMBRYO CULTURE

K002836 Class II Special
Decision Date
2000-10-03
Sponsor / Applicant
Sage Biopharma

Technical Specification

510(k) Submission ID K002836
Product Code MQL
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6180
Decision Date 2000-10-03
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDIA FOR GAMETE PREPARATION AND EMBRYO CULTURE received FDA 510(k) clearance under submission number K002836, sponsored by Sage Biopharma. 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 2000-10-03.

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.