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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Compressor, Air, Portable
510(k) Number K900686
Device Name MAXI COMPRESSORS
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 Number868.6250
Classification Product Code
BTI  
Date Received02/13/1990
Decision Date 04/26/1990
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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