Cleared Traditional

K211519 - Every Cycle Reusable Tampon Applicator (FDA 510(k) Clearance)

Aug 2021
Decision
88d
Days
Class 2
Risk

K211519 is an FDA 510(k) clearance for the Every Cycle Reusable Tampon Applicator. This device is classified as a Tampon, Menstrual, Unscented (Class II - Special Controls, product code HEB).

Submitted by Cycle, LLC (Santa Monica, US). The FDA issued a Cleared decision on August 13, 2021, 88 days after receiving the submission on May 17, 2021.

This device falls under the Obstetrics & Gynecology FDA review panel. Regulated under 21 CFR 884.5470. An Unscented Menstrual Tampon Is A Plug Made Of Cellulosic Or Synthetic Material That Is Inserted Into The Vagina And Used To Absorb Menstrual Fluid Or Other Vaginal Discharge..

Submission Details

510(k) Number K211519 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 17, 2021
Decision Date August 13, 2021
Days to Decision 88 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF

Device Classification

Product Code HEB - Tampon, Menstrual, Unscented
Device Class Class II - Special Controls
CFR Regulation 21 CFR 884.5470
Definition An Unscented Menstrual Tampon Is A Plug Made Of Cellulosic Or Synthetic Material That Is Inserted Into The Vagina And Used To Absorb Menstrual Fluid Or Other Vaginal Discharge.