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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Clamp, Vascular
510(k) Number K885161
Device Name VOSS VEIN CLAMP
Applicant
Voss Medical Products
7614 Louis Pasteur Dr.,
Suite 200
San Antonio,  TX  78229
Applicant Contact RON A VOSS
Correspondent
Voss Medical Products
7614 Louis Pasteur Dr.,
Suite 200
San Antonio,  TX  78229
Correspondent Contact RON A VOSS
Regulation Number870.4450
Classification Product Code
DXC  
Date Received12/13/1988
Decision Date 12/22/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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