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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 K791042
Device Name I.P.P.B. MANIFOLD & NEBULIZER, UNIVERSAL
Applicant
AIRLIFE, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
AIRLIFE, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent Contact - -
Regulation Number868.5630
Classification Product Code
CAF  
Date Received06/05/1979
Decision Date 06/13/1979
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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