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FDA 510(k) Applications Submitted by Jim Clossick
FDA 510(k) Number
Submission Date
Device Name
Applicant
K040550
03/02/2004
LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS
ORBUS MEDICAL TECHNOLOGIES
K221204
04/26/2022
Excipio SV Thrombectomy Device
Contego Medical Inc.
K221339
05/09/2022
Paladin Carotid Post-Dilation Balloon System with Integrated Embolic Protection
Contego Medical Inc.
K041370
05/24/2004
LIFESTENT LP SDS BILIARY ENDOPROSTHESIS
ORBUS MEDICAL TECHNOLOGIES
K023121
09/19/2002
LIFESTENT BILIARY ENDOPROSTHESIS
ORBUS MEDICAL TECHNOLOGIES
K023248
09/30/2002
LIFESTENT LP SDS BILIARY ENDOPROSTHESIS
ORBUS MEDICAL TECHNOLOGIES
K023308
10/03/2002
LIFESTENT SDS BILIARY ENDOPROSTHESIS, LIFESTENT XL SDS BILIARY ENDOPROSTHESIS
ORBUS MEDICAL TECHNOLOGIES
K033212
10/03/2003
LIFESTENT SDS BILIARY ENDOPROSTHESIS
ORBUS MEDICAL TECHNOLOGIES
K223897
12/28/2022
Excipio LV Thrombectomy Device
Contego Medical Inc.
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