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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
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