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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stripper, Vein, External
510(k) Number K872157
Device Name HALL VEIN STRIPPER
Applicant
Solco Basle, Inc.
Post Office Box 661
Wilton,  CT  06897
Applicant Contact J TURNER,PHD
Correspondent
Solco Basle, Inc.
Post Office Box 661
Wilton,  CT  06897
Correspondent Contact J TURNER,PHD
Regulation Number870.4885
Classification Product Code
DWQ  
Date Received06/04/1987
Decision Date 07/07/1987
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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