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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name circuit, breathing (w connector, adaptor, y piece)
510(k) Number K893919
Device Name ANTEC AIRWAY SAMPLING DEVICE W/MOISTURE TRAP
Applicant
BAXTER HEALTHCARE CORP.
27200 NORTH TOURNEY RD.
P.O. BOX 5900
VALENCIA,  CA  91355 -8900
Applicant Contact T MERRICK
Correspondent
BAXTER HEALTHCARE CORP.
27200 NORTH TOURNEY RD.
P.O. BOX 5900
VALENCIA,  CA  91355 -8900
Correspondent Contact T MERRICK
Regulation Number868.5240
Classification Product Code
CAI  
Date Received05/30/1989
Decision Date 09/15/1989
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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