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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name applier, aneurysm clip
510(k) Number K173271
Device Name Aesculap Slim Clip Applier Forceps
Applicant
Aesculap, Inc.
3773 Corporate Parkway
Center Valley,  PA  18034
Applicant Contact Paul Amudala
Correspondent
Aesculap, Inc.
3773 Corporate Parkway
Center Valley,  PA  18034
Correspondent Contact Paul Amudala
Regulation Number882.4175
Classification Product Code
HCI  
Date Received10/12/2017
Decision Date 11/10/2017
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
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