FDA 510(k) Applications Submitted by Michael 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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