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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