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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 K911880
Device Name ZEFON ADULT ANESTHESIA BREATHING CIRCUIT
Applicant
BILL OLSON CORP.
5350 S.W. FIRST LN.
OCALA,  FL  34474
Applicant Contact MICHAEL BYRNE
Correspondent
BILL OLSON CORP.
5350 S.W. FIRST LN.
OCALA,  FL  34474
Correspondent Contact MICHAEL BYRNE
Regulation Number868.5240
Classification Product Code
CAI  
Date Received04/29/1991
Decision Date 12/20/1991
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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