meddevicedb.com FDA Device Reference

SKIN LESS SKIN CONDOM W/SPERMICIDAL LUBRICANT

K884401 Class II Traditional
Decision Date
1989-01-12
Sponsor / Applicant
Okamoto USA, Inc.

Technical Specification

510(k) Submission ID K884401
Product Code HIS
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 1989-01-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SKIN LESS SKIN CONDOM W/SPERMICIDAL LUBRICANT received FDA 510(k) clearance under submission number K884401, sponsored by Okamoto 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 1989-01-12.

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.