meddevicedb.com FDA Device Reference

DB1 EMBRYO FREEZE

K011327 Class II Traditional
Decision Date
2002-08-15
Sponsor / Applicant
Zander Medical Supplies, Inc.

Technical Specification

510(k) Submission ID K011327
Product Code MQG
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6120
Decision Date 2002-08-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DB1 EMBRYO FREEZE received FDA 510(k) clearance under submission number K011327, sponsored by Zander Medical Supplies, Inc.. 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 2002-08-15.

Classification & Regulation

This clearance is catalogued under FDA product code MQG and 21 CFR 884.6120, within the Obstetrics/Gynecology review panel as a Class II device.