FDA 510(k) Applications Submitted by MEGHAN J TINTLE

FDA 510(k) Number Submission Date Device Name Applicant
K030270 01/27/2003 3F X 60 CM SINGLE LUMEN SILISONE VASCU-PICC, 4F X 60CM SINGLE LUMEN SILICONE VASCU-PICC, 5F X 60 CM SINGLE LUMEN SILICON MEDCOMP
K030502 02/19/2003 14.5F X 55CM HEMO-FLOW DOUBLE LUMEN CATHETER, MODELS HFS-55, HFT-55 MEDCOMP


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