FDA 510(k) Applications Submitted by BRYAN COWELL

FDA 510(k) Number Submission Date Device Name Applicant
K140042 01/08/2014 1.5MM HYDRO EXPANDABLE LEMAITRE VALVULOTOME LEMAITRE VASCULAR, INC.
K080711 03/13/2008 1.10-YEAR FRACTURE RISK QUESTIONNAIRE OPTION FOR QDR X-RAY BONE DENSITOMETER, MODEL QDR OPTION HOLOGIC, INC.
K111201 04/29/2011 C7 XR IMAGING SYSTEM LIGHTLAB IMAGING,INC.
K181533 06/11/2018 EVOS Wrist Fracture Plating System Smith & Nephew, Inc.
K072847 10/04/2007 APEX 2.0 SOFTWARE FOR QDR X-RAY BONE DENSITOMETERS HOLOGIC, INC.
K113584 12/05/2011 PRESSUREWIRE CERTUS, CERTUS 300, AERIS, AERIS 300, AND RECEIVER ST. JUDE MEDICAL
K123531 11/16/2012 UNBALLOON NON-OCCLUSIVE MODELING CATHETER LEMAITRE VASCULAR, INC.


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