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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Pump, Portable, Aspiration (Manual Or Powered)
510(k) Number K844200
Device Name K.M. PRODUCTS ASPIRATOR
Applicant
Km Products
1349 W. Allegheny
Tucson,  AZ  85705
Applicant Contact ALLAN R KENT
Correspondent
Km Products
1349 W. Allegheny
Tucson,  AZ  85705
Correspondent Contact ALLAN R KENT
Regulation Number878.4780
Classification Product Code
BTA  
Date Received10/30/1984
Decision Date 01/25/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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