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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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