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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 K902184
Device Name MAXI ASPIRATOR
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 Received05/14/1990
Decision Date 02/12/1991
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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