510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K924944Substantially Equivalent

Instant in-Dwell Nasal Suct Tamp/allevia Nasal Tra

Westmed Intl., Tucson AZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K924944 is the FDA 510(k) clearance record for INSTANT IN-DWELL NASAL SUCT TAMP/ALLEVIA NASAL TRA, a class I device, cleared for Westmed Intl. on under FDA product code EMX (Balloon, Epistaxis). FDA records list 9 510(k) clearances for Westmed Intl., from to . As of , FDA records show no recalls naming K924944.

Clearance record

Decision date
Received
(275 days to decision)
Product code
EMX Balloon, Epistaxis
Regulation
21 CFR 874.4100
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Westmed Intl. 3351 E. Hemisphere Loop, Tucson AZ
510(k) summary
Statement
Third party review
No

Clearances, product code EMX

Trailing 12 months

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

FDA records show no clearances under product code EMX in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EMX, 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