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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Regulator, Pressure, Gas Cylinder
510(k) Number K861166
Device Name OXYGEN THERAPY REGULATOR OR REGULATOR-FLOWMETER
Applicant
Victor
Suite 1000
1660 L St., NW
Washington,  DC  20036
Applicant Contact DAVID E MENOTTI
Correspondent
Victor
Suite 1000
1660 L St., NW
Washington,  DC  20036
Correspondent Contact DAVID E MENOTTI
Regulation Number868.2700
Classification Product Code
CAN  
Date Received03/28/1986
Decision Date 04/01/1986
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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