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FDA 510(k) Application Details - K143160
Device Classification Name
Catheters, Transluminal Coronary Angioplasty, Percutaneous
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510(K) Number
K143160
Device Name
Catheters, Transluminal Coronary Angioplasty, Percutaneous
Applicant
SHANGHAI MICROPORT MEDICAL (GROUP) CO., LTD
501 NEWTON ROAD
SHANGHAI 201203 CN
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Contact
JINGWEN LI
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Regulation Number
000.0000
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Classification Product Code
LOX
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More FDA Info for this Product Code
Date Received
11/03/2014
Decision Date
03/05/2015
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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