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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)
510(k) Number K941926
Device Name MEDI STRUMPF
Applicant
Medi USA, LP
76 W. Seegers Rd.
Arlington Heights,  IL  60005
Applicant Contact D. BRUCE GUYNN
Correspondent
Medi USA, LP
76 W. Seegers Rd.
Arlington Heights,  IL  60005
Correspondent Contact D. BRUCE GUYNN
Regulation Number880.5780
Classification Product Code
DWL  
Date Received04/20/1994
Decision Date 06/15/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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