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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Mask, Oxygen, Low Concentration, Venturi
510(k) Number K780626
Device Name VENTURI OXYGEN MASK
Applicant
Hospitak, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Hospitak, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number868.5600
Classification Product Code
BYF  
Date Received04/14/1978
Decision Date 05/26/1978
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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