Intelli-Ox— 510(k) K161179

Name: FDA 510(k) clearance K161179
Creator: U.S. Food and Drug Administration
Published: 2017-04-13

Substantially Equivalent

Air Liquide Healthcare America Corporation

FDA 510(k) clearance K161179 for Intelli-Ox, Substantially Equivalent on 2017-04-13. Applicant: Air Liquide Healthcare America Corporation. Device class: 1.

Clearance details

Applicant: Air Liquide Healthcare America Corporation
Product code: Code ECX
Device class: Class 1
Regulation: 21 CFR 868.2700
Advisory panel: Anesthesiology
Date received: 2016-04-26
Decision date: 2017-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code ECX

view all

K161472 — Walk-O2-Bout2016-11-18
K153518 — Medipure Oxygen-LC System2016-06-03
K143060 — Intelli-Ox2015-05-21
K142149 — OXYTOTE INFINITY SERIES VIPR SYSTEMS2015-04-17
K132778 — GRAB 'N GO PLUS, GRAB 'N GO DIGITAL2014-07-07

More clearances from Air Liquide Healthcare America Corporation

view all

K153564 — PURE CRYOGEN2016-03-29

Data sourced from openFDA. This site is unofficial and independent of the FDA.