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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Vaporizer, Anesthesia, Non-Heated
510(k) Number K843993
Device Name ANAESLOCK THREE VAPORIZER INTERLOCK HVA003
Applicant
Southmedic, Inc.
P.O. Box 7278
Ancaster, Ontario,  CA
Applicant Contact LEE MCDONALD
Correspondent
Southmedic, Inc.
P.O. Box 7278
Ancaster, Ontario,  CA
Correspondent Contact LEE MCDONALD
Regulation Number868.5880
Classification Product Code
CAD  
Date Received10/11/1984
Decision Date 11/15/1984
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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