meddevicedb.com FDA Device Reference

LifeStyles® HydraFeel Natural Rubber Latex Condom

K252521 Class II Abbreviated
Decision Date
2025-11-18
Sponsor / Applicant
Suretex Limited

Technical Specification

510(k) Submission ID K252521
Product Code HIS
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 2025-11-18
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LifeStyles® HydraFeel Natural Rubber Latex Condom received FDA 510(k) clearance under submission number K252521, sponsored by Suretex Limited. 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 2025-11-18.

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.