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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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