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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 K982371
Device Name MEDCO ASPIRATOR IV
Applicant
Medco Mfg.
8319 Thora #A1
Spring,  TX  77379
Applicant Contact ELAINE MARTIN
Correspondent
Medco Mfg.
8319 Thora #A1
Spring,  TX  77379
Correspondent Contact ELAINE MARTIN
Regulation Number878.4780
Classification Product Code
BTA  
Date Received07/07/1998
Decision Date 02/12/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Statement Statement
Type Abbreviated
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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