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FDA 510(k) Application Details - K201750
Device Classification Name
Catheter,Intracardiac Mapping,High-Density Array
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510(K) Number
K201750
Device Name
Catheter,Intracardiac Mapping,High-Density Array
Applicant
Biosense Webster, Inc
33 Technology Dr
Irvine, CA 92618 US
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Contact
Richard Lauhead
Other 510(k) Applications for this Contact
Regulation Number
870.1220
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Classification Product Code
MTD
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More FDA Info for this Product Code
Date Received
06/26/2020
Decision Date
08/06/2020
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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