510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K884090Substantially Equivalent

Lundy Vaporizer System

Vaporflow Technology, Inc., Tustin CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K884090 is the FDA 510(k) clearance record for LUNDY VAPORIZER SYSTEM, a class II device, cleared for Vaporflow Technology, Inc. on under FDA product code CAD (Vaporizer, Anesthesia, Non-Heated). FDA records list one 510(k) clearance for Vaporflow Technology, Inc. As of , FDA records show no recalls naming K884090.

Clearance record

Decision date
Received
(118 days to decision)
Product code
CAD Vaporizer, Anesthesia, Non-Heated
Regulation
21 CFR 868.5880
Device class
Class II
Review panel
Anesthesiology
Applicant
Vaporflow Technology, Inc. 1731 Saybrook Ln., Tustin CA
Third party review
No

Clearances, product code CAD

Trailing 12 months

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

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