meddevicedb.com FDA Device Reference

MALE NATURAL RUBBER LATEX CONDOM

K050244 Class II Abbreviated
Decision Date
2005-04-08
Sponsor / Applicant
Nrs Global Partners

Technical Specification

510(k) Submission ID K050244
Product Code HIS
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 2005-04-08
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MALE NATURAL RUBBER LATEX CONDOM received FDA 510(k) clearance under submission number K050244, sponsored by Nrs Global Partners. 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 2005-04-08.

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.