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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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