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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Surgical Instruments, G-U, Manual (And Accessories)
510(k) Number K932465
Device Name LI VASECTOMY
Applicant
Femcare , Ltd.
St. Peter'S St.
Nottingham
Ng7 3en England,  GB
Applicant Contact ANDREW MARTIN
Correspondent
Femcare , Ltd.
St. Peter'S St.
Nottingham
Ng7 3en England,  GB
Correspondent Contact ANDREW MARTIN
Regulation Number876.4730
Classification Product Code
KOA  
Date Received05/21/1993
Decision Date 03/02/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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