510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K861166Substantially Equivalent

Oxygen Therapy Regulator or Regulator-Flowmeter

Victor, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K861166 is the FDA 510(k) clearance record for OXYGEN THERAPY REGULATOR OR REGULATOR-FLOWMETER, a class I device, cleared for Victor on under FDA product code CAN (Regulator, Pressure, Gas Cylinder). FDA records list one 510(k) clearance for Victor. As of , FDA records show no recalls naming K861166.

Clearance record

Decision date
Received
(4 days to decision)
Product code
CAN Regulator, Pressure, Gas Cylinder
Regulation
21 CFR 868.2700
Device class
Class I
Review panel
Anesthesiology
Applicant
Victor Suite 1000, Washington DC
Third party review
No

Clearances, product code CAN

Trailing 12 months

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

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