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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 K925439
Device Name MICROSNARE
Applicant
Microvena Corp.
3600 Labore Rd. #1
Vadnais Heights,  MN  55110
Applicant Contact MICHAEL RENNER
Correspondent
Microvena Corp.
3600 Labore Rd. #1
Vadnais Heights,  MN  55110
Correspondent Contact MICHAEL RENNER
Regulation Number870.1250
Classification Product Code
DQY  
Date Received10/28/1992
Decision Date 09/24/1993
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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