FDA 510(k) Applications Submitted by DOUGLAS THISTLETHWAITE
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K160152 |
01/22/2016 |
Trillium Oval V 5.1 MRI System |
HITACHI MEDICAL SYSTEMS AMERICA, INC. |
K050307 |
02/08/2005 |
AIRIS ELITE RAPID BODY COIL |
HITACHI MEDICAL SYSTEMS AMERICA, INC. |
K040902 |
04/07/2004 |
HITACHI PRESTO |
HITACHI MEDICAL SYSTEMS AMERICA, INC. |
K001334 |
04/27/2000 |
HITACHI AIRIS II |
HITACHI MEDICAL SYSTEMS AMERICA, INC. |
K021751 |
05/28/2002 |
ALTAIRE MAGNETIC RESONANCE IMAGING SYSTEM |
HITACHI MEDICAL SYSTEMS AMERICA, INC. |
K071806 |
07/02/2007 |
ECLOS COMPUTED TOMOGRAPHY X-RAY SYSTEM |
HITACHI MEDICAL SYSTEMS AMERICA, INC. |
K061950 |
07/10/2006 |
HHF1 ECHELON MULTI-PURPOSE COIL |
HITACHI MEDICAL SYSTEMS AMERICA, INC. |
K032232 |
07/21/2003 |
AIRIS ELITE MAGNETIC RESONANCE IMAGING DEVICE |
HITACHI MEDICAL SYSTEMS AMERICA, INC. |
K022390 |
07/23/2002 |
HITACHI ALTAIRE |
HITACHI MEDICAL SYSTEMS AMERICA, INC. |
K002420 |
08/08/2000 |
HITACHI ALTAIRE |
HITACHI MEDICAL SYSTEMS AMERICA, INC. |
K994378 |
12/27/1999 |
AIRIS II |
HITACHI MEDICAL SYSTEMS AMERICA, INC. |
K042428 |
09/08/2004 |
SCEPTREP3 PET/CT |
HITACHI MEDICAL SYSTEMS AMERICA, INC. |
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