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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Nebulizer (Direct Patient Interface)
510(k) Number K063716
Device Name AEROSOL SYSTEM
Applicant
AMICI, INC.
518 VINCENT ST.
SPRING CITY,  PA  19475
Applicant Contact MICHAEL BONO
Correspondent
AMICI, INC.
518 VINCENT ST.
SPRING CITY,  PA  19475
Correspondent Contact MICHAEL BONO
Regulation Number868.5630
Classification Product Code
CAF  
Date Received12/14/2006
Decision Date 12/28/2007
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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