Cleared Traditional

K212277 - Tempo Tampon (FDA 510(k) Clearance)

Apr 2022
Decision
275d
Days
Class 2
Risk

K212277 is an FDA 510(k) clearance for the Tempo Tampon. This device is classified as a Tampon, Menstrual, Unscented (Class II - Special Controls, product code HEB).

Submitted by Dong-A Pharmaceutical Co., Ltd. (Seoul, KR). The FDA issued a Cleared decision on April 21, 2022, 275 days after receiving the submission on July 20, 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 K212277 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 20, 2021
Decision Date April 21, 2022
Days to Decision 275 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.