FDA 510(k) Applications Submitted by JEFFREY P DUMONTELLE

FDA 510(k) Number Submission Date Device Name Applicant
K200314 02/06/2020 Capere Thrombectomy System Vascular Medcure, Inc.
K070488 02/20/2007 MICARDIA ANNULOPLASTY BAND DR MICARDIA CORPORATION
K192935 10/17/2019 CAPERE Thrombectomy System Vascular Medcure, Inc.
K201216 05/05/2020 CAPERE Thrombectomy System Vascular Medcure, Inc.
K183179 11/16/2018 CAPERE Thrombectomy System Vascular Medcure, Inc.
K203476 11/25/2020 CAPERE Thrombectomy System Vascular Medcure, INC.


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