DeviceClearance

Product code NUQ— Obstetrics/Gynecology

LUNAPADS

Classification name
Pad, Menstrual, Reusable
Device class
Class 1
Regulation
21 CFR 884.5435
Advisory panel
Obstetrics/Gynecology
Total cleared
1
First cleared
Most recent

FDA classification 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.”

— U.S. Food and Drug Administration, device classification record for product code NUQ under 21 CFR 884.5435, via openFDA

Market context for product code NUQ

FDA has cleared 1 device under product code NUQ, all in 2001, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Top applicants under product code NUQ

Recent clearances under product code NUQ

Data sourced from openFDA. This site is unofficial and independent of the FDA.