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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 K924889
Device Name ZEFON ADULT ANESTHESIA BREATHING CIRCUIT
Applicant
ZEFON MEDICAL PRODUCTS
5350 SOUTHWEST FIRST LN.
OCALA,  FL  34474
Applicant Contact JOSEPH BOZOSI
Correspondent
ZEFON MEDICAL PRODUCTS
5350 SOUTHWEST FIRST LN.
OCALA,  FL  34474
Correspondent Contact JOSEPH BOZOSI
Regulation Number868.5240
Classification Product Code
CAI  
Date Received09/28/1992
Decision Date 03/19/1993
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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