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ENHANCE HTF MEDIUM WITH HEPES

K023655 Class II Traditional
Decision Date
2002-12-13
Sponsor / Applicant
Conception Technologies

Technical Specification

510(k) Submission ID K023655
Product Code MQL
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6180
Decision Date 2002-12-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENHANCE HTF MEDIUM WITH HEPES received FDA 510(k) clearance under submission number K023655, sponsored by Conception Technologies. 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 2002-12-13.

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.