FDA 510(k) Applications Submitted by INJECTIMED, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K040029 01/08/2004 SAFETYNET GUIDEWIRE INTRODUCER INJECTIMED, INC.
K073664 12/26/2007 FRONTLINE MEDICAL SAFETYNET GUIDEWIRE INTRODUCER INJECTIMED, INC.


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