FDA 510(k) Applications Submitted by C-RAD POSITIONING AB

FDA 510(k) Number Submission Date Device Name Applicant
K063839 12/26/2006 POSITIONER C-RAD POSITIONING AB
K082582 09/08/2008 SENTINEL, MODEL SP-001 C-RAD POSITIONING AB
K120668 03/05/2012 SENTINEL C-RAD POSITIONING AB
K113276 11/07/2011 CATALYST C-RAD POSITIONING AB
K200435 02/24/2020 Catalyst+, Catalyst+ HD C-Rad Positioning AB
K200600 03/09/2020 Sentinel C-Rad Positioning AB


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