510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K832220Substantially Equivalent

Traveler Nebulizing System

Medix of Florida, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K832220 is the FDA 510(k) clearance record for TRAVELER NEBULIZING SYSTEM, a class II device, cleared for Medix of Florida, Inc. on under FDA product code BTI (Compressor, Air, Portable). FDA records list one 510(k) clearance for Medix of Florida, Inc. As of , FDA records show no recalls naming K832220.

Clearance record

Decision date
Received
(80 days to decision)
Product code
BTI Compressor, Air, Portable
Regulation
21 CFR 868.6250
Device class
Class II
Review panel
Anesthesiology
Applicant
Medix of Florida, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code BTI

Trailing 12 months

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

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