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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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