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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name apparatus, nitric oxide delivery
510(k) Number K000653
Device Name AERONOX UNIVERSAL, MODEL P/N 360000, AERONOX BEDSIDE, MODEL P/N 360001, AERONOX TRANSPORT TRANSPORT, MODEL P/N 360002
Applicant
PULMONOX MEDICAL CORP.
5243-53 AVE.
TOFIELD, ALBERTA,  CA T0B 4J0
Applicant Contact PAULA TOMAT
Correspondent
PULMONOX MEDICAL CORP.
5243-53 AVE.
TOFIELD, ALBERTA,  CA T0B 4J0
Correspondent Contact PAULA TOMAT
Regulation Number868.5165
Classification Product Code
MRN  
Subsequent Product Codes
MRO   MRP   MRQ  
Date Received02/28/2000
Decision Date 08/04/2000
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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