meddevicedb.com FDA Device Reference

BESTCON/LUBRICATED CONDOMS

K871470 Class II Traditional
Decision Date
1987-08-05
Sponsor / Applicant
Europharmaceutical Corp.

Technical Specification

510(k) Submission ID K871470
Product Code HIS
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 1987-08-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BESTCON/LUBRICATED CONDOMS received FDA 510(k) clearance under submission number K871470, sponsored by Europharmaceutical Corp.. 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 1987-08-05.

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.