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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Catheter, Percutaneous
510(k) Number K834232
Device Name VAS-CATH DSA CATHETER/TRAY
Applicant
VAS-CATH OF CANADA LTD.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
VAS-CATH OF CANADA LTD.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number870.1250
Classification Product Code
DQY  
Date Received12/06/1983
Decision Date 04/24/1984
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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