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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name ventilator, continuous, facility use
510(k) Number K990429
Device Name MODIFICATION OF VENTURI VENTILATOR
Applicant
CARDIOPULMONARY CORP.
200 CASCADE BLVD.
MILFORD,  CT  06460
Applicant Contact JOHN LAVIOLA
Correspondent
CARDIOPULMONARY CORP.
200 CASCADE BLVD.
MILFORD,  CT  06460
Correspondent Contact JOHN LAVIOLA
Regulation Number868.5895
Classification Product Code
CBK  
Date Received02/11/1999
Decision Date 02/24/1999
Decision SE SUBJECT TO TRACKING REG (ST)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
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