meddevicedb.com FDA Device Reference

TROJAN MINT TINGLE BRAND LATEX CONDOMS

K023405 Class II Abbreviated
Decision Date
2002-12-16
Sponsor / Applicant
Armkel, LLC

Technical Specification

510(k) Submission ID K023405
Product Code HIS
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 2002-12-16
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TROJAN MINT TINGLE BRAND LATEX CONDOMS received FDA 510(k) clearance under submission number K023405, sponsored by Armkel, LLC. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2002-12-16.

Classification & Regulation

This clearance is catalogued under FDA product code HIS and 21 CFR 884.5300, within the Obstetrics/Gynecology review panel as a Class II device.