510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902906Substantially Equivalent

Gas-Vak(r) Combination Sterilizer & Ventilator

Gas-Vak, Westwood CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902906 is the FDA 510(k) clearance record for GAS-VAK(R) COMBINATION STERILIZER & VENTILATOR, a class II device, cleared for Gas-Vak on under FDA product code FLI (Cabinet, Ethylene-Oxide Gas Aerator). FDA records list 2 510(k) clearances for Gas-Vak, from to . As of , FDA records show no recalls naming K902906.

Clearance record

Decision date
Received
(104 days to decision)
Product code
FLI Cabinet, Ethylene-Oxide Gas Aerator
Regulation
21 CFR 880.6100
Device class
Class II
Review panel
General Hospital
Applicant
Gas-Vak P.O. Box 941, Westwood CA
Third party review
No

Clearances, product code FLI

Trailing 12 months

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

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