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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 K883790
Device Name SURGICAL CLAMP INSERTS
Applicant
APPLIED VASCULAR DEVICES, INC.
2740 S. HARBOR, SUITE K
SANTA ANA,  CA  92704
Applicant Contact SAID S HILAL
Correspondent
APPLIED VASCULAR DEVICES, INC.
2740 S. HARBOR, SUITE K
SANTA ANA,  CA  92704
Correspondent Contact SAID S HILAL
Regulation Number870.4450
Classification Product Code
DXC  
Date Received09/07/1988
Decision Date 12/27/1988
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
Recalls CDRH Recalls
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