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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Clamp, Surgical, General & Plastic Surgery
510(k) Number K881741
Device Name STUART LEE CLIP
Applicant
Stuart-Lee, Inc.
41 Trumbull Rd.
Waterford,  CT  06385
Applicant Contact VAUGHN DURHAM
Correspondent
Stuart-Lee, Inc.
41 Trumbull Rd.
Waterford,  CT  06385
Correspondent Contact VAUGHN DURHAM
Regulation Number878.4800
Classification Product Code
GDJ  
Date Received04/22/1988
Decision Date 06/03/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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