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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Unit, Liquid-Oxygen, Portable
510(k) Number K863205
Device Name SWIVEL COUPLER
Applicant
Venmill Swivel, Co.
29 Carlton St.
Methuen,  MA  01844
Applicant Contact RICHARD G MILLER,JR
Correspondent
Venmill Swivel, Co.
29 Carlton St.
Methuen,  MA  01844
Correspondent Contact RICHARD G MILLER,JR
Regulation Number868.5655
Classification Product Code
BYJ  
Date Received08/19/1986
Decision Date 10/02/1986
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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