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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Prosthesis, Penile
510(k) Number K910214
Device Name AMS 700 ULTREX(TM) PRECONNECTED PENILE PROSTHESIS
Applicant
American Medical Corp.
11001 Bren Rd. E.
Minnetonka,  MN  55343
Applicant Contact QUINLAN SMITH
Correspondent
American Medical Corp.
11001 Bren Rd. E.
Minnetonka,  MN  55343
Correspondent Contact QUINLAN SMITH
Regulation Number876.3630
Classification Product Code
FAE  
Date Received01/17/1991
Decision Date 04/25/1991
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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