510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K890144Substantially Equivalent

Oxitron Oxygen Sensor

Oxitron Medical Products, Chatsworth CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K890144 is the FDA 510(k) clearance record for OXITRON OXYGEN SENSOR, a class II device, cleared for Oxitron Medical Products on under FDA product code CCL (Analyzer, Gas, Oxygen, Gaseous-Phase). FDA records list 2 510(k) clearances for Oxitron Medical Products, from to . As of , FDA records show no recalls naming K890144.

Clearance record

Decision date
Received
(132 days to decision)
Product code
CCL Analyzer, Gas, Oxygen, Gaseous-Phase
Regulation
21 CFR 868.1720
Device class
Class II
Review panel
Anesthesiology
Applicant
Oxitron Medical Products 8967 Oso Ave., Chatsworth CA
Third party review
No

Clearances, product code CCL

Trailing 12 months
1 clearance under product code CCL in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CCL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260