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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Conserver, Oxygen
510(k) Number K890298
Device Name DEMAND NASAL OXYGEN CANNULA MODELS 4008/4108/4208
Applicant
Salter Labs
P.O. Box 608
Arvin,  CA  93203
Applicant Contact JAMES N CURTI
Correspondent
Salter Labs
P.O. Box 608
Arvin,  CA  93203
Correspondent Contact JAMES N CURTI
Regulation Number868.5905
Classification Product Code
NFB  
Date Received01/19/1989
Decision Date 02/23/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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