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 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
- 2018
- 2012
- 2004
- 1998
- 1997
- 1996
- 1995
- 1993
- 1991
- 1988
- 1987
- 1986
Top applicants under product code LWF
Recent clearances under product code LWF
- K181219 — OptiPillows EPAP Mask
- K120665 — INVENT SNORING DEVICE
- K040491 — CHIN-UP STRIP
- K982929 — MAXAIR NASAL DILATOR SYSTEM
- K963326 — BREATHE FIT
- K962400 — AIR MAX EXTERNAL NASAL DILATOR STRIP
- K962698 — ACUTEK'S CLEARPASAGE
- K955711 — BREATHE RIGHT NASAL STRIP
- K954914 — BREATHE RIGHT NASAL STRIP
- K955233 — EASY BREATHING NASAL STRIPS
- K953042 — E-Z BREATHERS
- K942025 — BURGET NASAL STENT
- K953772 — BREATHE RIGHT NASAL STRIP
- K954252 — EASY BREATHING NASAL STRIPS
- K951644 — ACUTEK'S CLEARPASSAGE
- K921220 — BREATHE RIGHT
- K904290 — NOZOVENT, NASAL DILATOR
- K882131 — NOSE BRACE
- K874089 — BREATHE WITH EEZ (NASAL DILATOR)
- K862406 — NOZEES NOSTRIL DILATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.