Cleared Traditional

K201003 - Callaly Tampliner (FDA 510(k) Clearance)

Dec 2020
Decision
235d
Days
Class 2
Risk

K201003 is an FDA 510(k) clearance for the Callaly Tampliner. This device is classified as a Tampon, Menstrual, Unscented (Class II - Special Controls, product code HEB).

Submitted by Calla Lily Personal Care, Ltd. (London, GB). The FDA issued a Cleared decision on December 7, 2020, 235 days after receiving the submission on April 16, 2020.

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 K201003 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 16, 2020
Decision Date December 07, 2020
Days to Decision 235 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Statement

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.