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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 K935494
Device Name DANESHVAR'S DEVICE
Applicant
Y. Daneshvar
33433 Six Mile Rd.
Livonia,  MI  48152
Applicant Contact Y. DANESHVAR
Correspondent
Y. Daneshvar
33433 Six Mile Rd.
Livonia,  MI  48152
Correspondent Contact Y. DANESHVAR
Regulation Number870.4450
Classification Product Code
DXC  
Date Received11/15/1993
Decision Date 11/22/1994
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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