Cleared Special

K133244 - TAMPAX M PLASTIC TAMPONS, UNSCENTED (FDA 510(k) Clearance)

Jan 2014
Decision
79d
Days
Class 2
Risk

K133244 is an FDA 510(k) clearance for the TAMPAX M PLASTIC TAMPONS, UNSCENTED. This device is classified as a Tampon, Menstrual, Unscented (Class II - Special Controls, product code HEB).

Submitted by The Procter & Gamble Company (Cincinnati, US). The FDA issued a Cleared decision on January 9, 2014, 79 days after receiving the submission on October 22, 2013.

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 K133244 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 22, 2013
Decision Date January 09, 2014
Days to Decision 79 days
Submission Type Special
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.