meddevicedb.com FDA Device Reference

ALLGRAD WASH (HERPES BUFFERED WASHING MEDIUM)

K023033 Class II Traditional
Decision Date
2002-11-26
Sponsor / Applicant
<Genx> Intl., Inc.

Technical Specification

510(k) Submission ID K023033
Product Code MQL
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.6180
Decision Date 2002-11-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALLGRAD WASH (HERPES BUFFERED WASHING MEDIUM) received FDA 510(k) clearance under submission number K023033, sponsored by <Genx> Intl., 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 2002-11-26.

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.