meddevicedb.com FDA Device Reference

EXTRA STRENGTH SKIN LESS SKIN CONDOM

K884402 Class II Traditional
Decision Date
1989-03-10
Sponsor / Applicant
Okamoto USA, Inc.

Technical Specification

510(k) Submission ID K884402
Product Code HIS
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 1989-03-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXTRA STRENGTH SKIN LESS SKIN CONDOM received FDA 510(k) clearance under submission number K884402, 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 1989-03-10.

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.