510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K833326Substantially Equivalent

Mini Ox III Oxygen Monitor

Catalyst Research Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K833326 is the FDA 510(k) clearance record for MINI OX III OXYGEN MONITOR, a class I device, cleared for Catalyst Research Corp. on under FDA product code BXL (Algesimeter, Manual). FDA records list 9 510(k) clearances for Catalyst Research Corp., from to . As of , FDA records show no recalls naming K833326.

Clearance record

Decision date
Received
(37 days to decision)
Product code
BXL Algesimeter, Manual
Regulation
21 CFR 868.1030
Device class
Class I
Review panel
Anesthesiology
Applicant
Catalyst Research Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code BXL

Trailing 12 months

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

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