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FDA 510(k) Application Details - K970668
Device Classification Name
Catheter, Percutaneous
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510(K) Number
K970668
Device Name
Catheter, Percutaneous
Applicant
MICROVENA CORP.
1861 BUERKLE RD.
WHITE BEAR LAKE, MN 55110-5426 US
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Contact
KAREN BANNICK
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Regulation Number
870.1250
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Classification Product Code
DQY
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More FDA Info for this Product Code
Date Received
02/24/1997
Decision Date
06/10/1998
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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