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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 K923265
Device Name FUNNEL ADAPTOR
Applicant
SOUTHMEDIC, INC.
P.O. BOX 1365
BARRIE, ONTARIO CANADA,  CA L4M 5R4
Applicant Contact PAUL E DRYDEN
Correspondent
SOUTHMEDIC, INC.
P.O. BOX 1365
BARRIE, ONTARIO CANADA,  CA L4M 5R4
Correspondent Contact PAUL E DRYDEN
Regulation Number868.5880
Classification Product Code
CAD  
Date Received07/02/1992
Decision Date 03/18/1993
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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