510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K955233Substantially Equivalent

Easy Breathing Nasal Strips

Corbett Lair, Inc., Portland OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K955233 is the FDA 510(k) clearance record for EASY BREATHING NASAL STRIPS, a class I device, cleared for Corbett Lair, Inc. on under FDA product code LWF (Dilator, Nasal). FDA records list 2 510(k) clearances for Corbett Lair, Inc., from to . As of , FDA records show no recalls naming K955233.

Clearance record

Decision date
Received
(37 days to decision)
Product code
LWF Dilator, Nasal
Regulation
21 CFR 874.3900
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Corbett Lair, Inc. 3926 SW Water Ave., Portland OR
510(k) summary
Statement
Third party review
No

Clearances, product code LWF

Trailing 12 months

FDA records hold no clearances under product code LWF in the trailing twelve months.

FDA records show no clearances under product code LWF in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LWF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260