FDA 510(k) Applications Submitted by MICHAEL J LEIGH

FDA 510(k) Number Submission Date Device Name Applicant
K010074 01/09/2001 MODEL 455GE PHASED ARRAY WRIST COIL MEDICAL ADVANCES, INC.
K110179 01/21/2011 INCONTROL INCONTROL MEDICAL, LLC
K160350 02/08/2016 ECG CT Gating Device NEOCOIL, LLC
K141832 07/07/2014 3T 16CH FLEX SPEEDER, MEDIUM , 3T 16CH FLEX SPEEDER, LARGE NEOCOIL, LLC
K072272 08/15/2007 HONEYWELL HOMMED CENTRAL STATION 4.0 HONEYWELL HOMMED, LLC
K173377 10/30/2017 3.0T 16ch Breast Coil NeoCoil, LLC
K173409 11/01/2017 Wireless Audio System NeoCoil, LLC
K003685 11/30/2000 MODEL 342GE-64 HIGH RESOLUTION BRAIN COIL MEDICAL ADVANCES, INC.
K120320 02/02/2012 CONNECTED CARE CLINICAL APPLICATION WATERMARK MEDICAL INC
K120325 02/02/2012 CONNECTED CARE MOBILE APPLICATION WATERMARK MEDICAL
K120470 02/16/2012 MIPAL WATERMARK MEDICAL
K011608 05/25/2001 MODEL 235GE-64; MULTI PURPOSE FLEX ARRAY COIL MEDICAL ADVANCES, INC.
K003366 10/30/2000 MODEL 545PH SERIES: PHASED ARRAY MUSCULO-SKELETAL FLEX COIL IGC-MEDICAL ADVANCES, INC.


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