NUQ — Pad, Menstrual, Reusable Class I

FDA Device Classification

FDA product code NUQ covers "Pad, Menstrual, Reusable", a Class I medical device regulated under 21 CFR 884.5435. Submissions are reviewed by the Obstetrics/Gynecology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
NUQ
Device Class
Class I
Regulation Number
884.5435
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No

Definition

A reusable, unscented menstrual pad which is used to absorb menstrual fluid or other vaginal discharge and is made of common cellulosic or synthetic material with an established safety profile.

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K010986lunapads international productsLUNAPADSJune 13, 2001