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
K131990Substantially Equivalent

Oxygen Generator Liquefier - (Ogl)

Essex Cryogenics of Missouri, Inc., St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K131990 is the FDA 510(k) clearance record for OXYGEN GENERATOR LIQUEFIER - (OGL), a class II device, cleared for Essex Cryogenics of Missouri, Inc. on under FDA product code CAW (Generator, Oxygen, Portable). FDA records list 5 510(k) clearances for Essex Cryogenics of Missouri, Inc., from to . As of , FDA records show no recalls naming K131990.

Clearance record

Decision date
Received
(238 days to decision)
Product code
CAW Generator, Oxygen, Portable
Regulation
21 CFR 868.5440
Device class
Class II
Review panel
Anesthesiology
Applicant
Essex Cryogenics of Missouri, Inc. 8007 Chivvis Dr., St. Louis MO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code CAW

Trailing 12 months
12 clearances under product code CAW in the twelve months to October 2026, December 2025 the highest month at 5.
Show the numbers
Monthly 510(k) clearances under FDA product code CAW, trailing twelve months
MonthClearances
November 20251
December 20255
January 20260
February 20260
March 20261
April 20261
May 20261
June 20261
July 20260
August 20261
September 20261
October 20260