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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Clamp, Vascular
510(k) Number K761169
Device Name GRANT MODIF OF DEBAKEY ABDOM AORTA CLMP
Applicant
Pilling Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Pilling Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number870.4450
Classification Product Code
DXC  
Date Received12/01/1976
Decision Date 12/09/1976
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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