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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 STREET, N.W.
WASHINGTON,  DC  20036
Applicant Contact DAVID E MENOTTI
Correspondent
VICTOR
SUITE 1000
1660 L STREET, N.W.
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
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