510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K822328Substantially Equivalent

Il 301 Transcutaneous Oxygen Monitor

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

K822328 is the FDA 510(k) clearance record for IL 301 TRANSCUTANEOUS OXYGEN MONITOR, a class II device, cleared for Instrumentation Laboratory CO on under FDA product code KLK (Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia). FDA records list 327 510(k) clearances for Instrumentation Laboratory CO, from to . As of , FDA records show no recalls naming K822328.

Clearance record

Decision date
Received
(35 days to decision)
Product code
KLK Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia
Regulation
21 CFR 868.2500
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 KLK

Trailing 12 months

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

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