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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 K922971
Device Name NO-SCALPEL VASCETOMY INSTRUMENTS
Applicant
Pilling Co.
420 Delaware Dr.
Fort Washington,  PA  19034
Applicant Contact RICHARD G JONES
Correspondent
Pilling Co.
420 Delaware Dr.
Fort Washington,  PA  19034
Correspondent Contact RICHARD G JONES
Regulation Number876.4730
Classification Product Code
KOA  
Date Received06/19/1992
Decision Date 09/23/1992
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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