510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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NUQClass I

Pad, Menstrual, Reusable

21 CFR 884.5435 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

NUQ is the FDA product code for Pad, Menstrual, Reusable, a class I device type, regulated under 21 CFR 884.5435. FDA's definition for this code reads: "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". As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
NUQ
Device name
Pad, Menstrual, Reusable
FDA 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.
Regulation
21 CFR 884.5435
Device class
Class I
Review panel
Obstetrics/Gynecology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code NUQ

By decision year
1 clearance under product code NUQ with a decision year between 2001 and 2001, 2001 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NUQ by decision year
YearClearances
20011

Applicants with the most clearances

Product code NUQ
Applicants holding the most 510(k) clearances under product code NUQ
ApplicantClearances
Lunapads International Products, Ltd.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 81 companies shown, in name order