FDA 510(k) Applications Submitted by Joel Tuckey
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K070542 |
02/26/2007 |
CARDIUS 1, 2 AND 3 XPO AND 2020TC SPECT IMAGING SYSTEMS |
DIGIRAD CORP. |
K100838 |
03/24/2010 |
ERGO IMAGING SYSTEM |
DIGIRAD CORP. |
K051549 |
06/13/2005 |
CARDIUS-1, CARDIUS-2, CARDIUS-3, 2020TC SPECT IMAGING SYSTEM |
DIGIRAD CORP. |
K082368 |
08/18/2008 |
CARDIUS-1, -2, -3, AND CARDIUS 1,2,3 XPO SPECT IMAGING SYSTEMS, 2020TC SPECT IMAGING SYSTEM |
DIGIRAD CORP. |
K052430 |
09/06/2005 |
CARDIUS-1, CARDIUS-2, CARDIUS-3, 2020TC SPECT IMAGING SYSTEM |
DIGIRAD CORP. |
K082904 |
09/30/2008 |
STASYS MOTION CORRECTION SOFTWARE |
DIGIRAD CORP. |
K083649 |
12/09/2008 |
CARDIUS 3 X-ACT |
DIGIRAD CORP. |
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