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FDA 510(k) Application Details - K150631
Device Classification Name
Catheter, Electrode Recording, Or Probe, Electrode Recording
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510(K) Number
K150631
Device Name
Catheter, Electrode Recording, Or Probe, Electrode Recording
Applicant
St. Jude Medical
14901 De Veau Place
Minnetonka, MN 55345-2126 US
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Contact
Harlan Jones
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Regulation Number
870.1220
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Classification Product Code
DRF
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More FDA Info for this Product Code
Date Received
03/11/2015
Decision Date
04/01/2015
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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