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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 K842708
Device Name MED. SUPPORT STOCKING-VENOFIT LASTOFLEX
Applicant
Kundt + Co. AG
One Farragut Sq. South
Washington,  DC  20006
Applicant Contact LOTHAR GRIESSBAC
Correspondent
Kundt + Co. AG
One Farragut Sq. South
Washington,  DC  20006
Correspondent Contact LOTHAR GRIESSBAC
Regulation Number880.5780
Classification Product Code
DWL  
Date Received07/12/1984
Decision Date 10/09/1984
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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