510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K823374Substantially Equivalent

Oxygen Monitor Il 408

Instrumentation Laboratory Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K823374 is the FDA 510(k) clearance record for OXYGEN MONITOR IL 408, a class II device, cleared for Instrumentation Laboratory CO on under FDA product code CCL (Analyzer, Gas, Oxygen, Gaseous-Phase). FDA records list 327 510(k) clearances for Instrumentation Laboratory CO, from to . As of , FDA records show no recalls naming K823374.

Clearance record

Decision date
Received
(27 days to decision)
Product code
CCL Analyzer, Gas, Oxygen, Gaseous-Phase
Regulation
21 CFR 868.1720
Device class
Class II
Review panel
Anesthesiology
Applicant
Instrumentation Laboratory CO 803 N. Front St. Suite 3, Mchenry IL
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