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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name cylinder, compressed gas, and valve
510(k) Number K143060
Device Name Intelli-Ox
Applicant
AIR LIQUIDE HEALTHCARE
2700 POST OAK BLVD., SUITE 325
HOUSTON,  TX  77056
Applicant Contact ANGIE BEYER
Correspondent
AIR LIQUIDE HEALTHCARE
2700 POST OAK BLVD., SUITE 325
HOUSTON,  TX  77056
Correspondent Contact ANGIE BEYER
Regulation Number868.2700
Classification Product Code
ECX  
Date Received10/24/2014
Decision Date 05/21/2015
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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