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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
Recalls CDRH Recalls
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