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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Laparoscope, General & Plastic Surgery
510(k) Number K923726
Device Name KENSEY NASH DYNAMIC CLIP SYSTEM
Applicant
KENSEY NASH CORP.
55 EAST UWCHLAN AVE.
MARSH CREEK CORP. CENTER
EXTON,  PA  19341 -1247
Applicant Contact SPRIEGEL
Correspondent
KENSEY NASH CORP.
55 EAST UWCHLAN AVE.
MARSH CREEK CORP. CENTER
EXTON,  PA  19341 -1247
Correspondent Contact SPRIEGEL
Regulation Number876.1500
Classification Product Code
GCJ  
Date Received07/27/1992
Decision Date 04/06/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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