FDA 510(k) Applications Submitted by INTERRAD MEDICAL, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K092306 07/29/2009 SECURACATH UNIVERSAL INTERRAD MEDICAL, INC.
K082047 07/18/2008 SECURACATH CATHETER, MODEL SPK01 INTERRAD MEDICAL, INC.
K083081 10/16/2008 MODIFICATION TO SECURACATH, MODEL: SPK01 INTERRAD MEDICAL, INC.


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