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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 K903499
Device Name MINI-MICRON CIRCUIT
Applicant
Medical Industries America, Inc.
2875 R Ave.
Adel,  IA  50003
Applicant Contact RUSSELL F BIRD
Correspondent
Medical Industries America, Inc.
2875 R Ave.
Adel,  IA  50003
Correspondent Contact RUSSELL F BIRD
Regulation Number868.5630
Classification Product Code
CAF  
Date Received08/03/1990
Decision Date 03/27/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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