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FDA 510(k) Applications Submitted by Harlan Jones
FDA 510(k) Number
Submission Date
Device Name
Applicant
K150631
03/11/2015
St. Jude Medical MediGuide Enabled Livewire Steerable Electroohysiology Catheter, Livewire Electrophysiology Catheter
St. Jude Medical
K112103
07/22/2011
INTERLOCK-35 FIBERED IDC OCCLUSION SYSTEM
BOSTON SCIENTIFIC CORP.
K122587
08/24/2012
BRK TRANSSEPTAL NEEDLE MODEL 407200, 407201, 407205, 407206, 407207, G407208
ST. JUDE MEDICAL
K113651
12/12/2011
INTERLOCK-35 FIBERED IDC OCCLUSION SYSTEM
Boston Scientific Corporation
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