meddevicedb.com FDA Device Reference

Every Cycle Reusable Tampon Applicator

K211519 Class II Traditional
Decision Date
2021-08-13
Sponsor / Applicant
Cycle, LLC

Technical Specification

510(k) Submission ID K211519
Product Code HEB
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5470
Decision Date 2021-08-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Every Cycle Reusable Tampon Applicator received FDA 510(k) clearance under submission number K211519, sponsored by Cycle, LLC. 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 2021-08-13.

Classification & Regulation

This clearance is catalogued under FDA product code HEB and 21 CFR 884.5470, within the Obstetrics/Gynecology review panel as a Class II device.