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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 K951729
Device Name MEDI - PUMP
Applicant
Thomas Industries
1419 Illinois Ave.
Sheboygan,  WI  53082
Applicant Contact DAN P FISTER
Correspondent
Thomas Industries
1419 Illinois Ave.
Sheboygan,  WI  53082
Correspondent Contact DAN P FISTER
Regulation Number878.4780
Classification Product Code
BTA  
Date Received04/14/1995
Decision Date 08/21/1995
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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