Product code LWF— Ear, Nose, Throat

BREATHE RIGHT NASAL STRIP

Classification name
Dilator, Nasal
Device class
Class 1
Regulation
21 CFR 874.3900
Advisory panel
Ear, Nose, Throat
Total cleared
20
First cleared
Most recent

Market context for product code LWF

FDA has cleared 20 devices under product code LWF between 1986 and 2018, filed by 15 applicant companies. 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.

Clearances per year

Top applicants under product code LWF

Recent clearances under product code LWF

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