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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 K926055
Device Name THE MILLER NEBULIZER SYSTEM
Applicant
WARREN C. MILLER
405 BLOSSOM ST.
SUITE B
HOUSTON,  TX  77055
Applicant Contact CHARLES S BOYD
Correspondent
WARREN C. MILLER
405 BLOSSOM ST.
SUITE B
HOUSTON,  TX  77055
Correspondent Contact CHARLES S BOYD
Regulation Number868.5630
Classification Product Code
CAF  
Date Received11/05/1992
Decision Date 02/03/1993
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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