meddevicedb.com FDA Device Reference

SPERMICIDAL LUBRICATED CONDOM

K931220 Class II Traditional
Decision Date
1996-05-22
Sponsor / Applicant
Monsys USA, Inc.

Technical Specification

510(k) Submission ID K931220
Product Code LTZ
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5310
Decision Date 1996-05-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPERMICIDAL LUBRICATED CONDOM received FDA 510(k) clearance under submission number K931220, sponsored by Monsys USA, 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 1996-05-22.

Classification & Regulation

This clearance is catalogued under FDA product code LTZ and 21 CFR 884.5310, within the Obstetrics/Gynecology review panel as a Class II device.