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FDA 510(k) Applications Submitted by EDDIE MONROE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990173
01/19/1999
PATHFINDER II ANGIOGRAPHIC CATHETER
MAXXIM MEDICAL
K984189
11/23/1998
ARGON MULTI-LUMEN CENTRAL VENOUS CATHETER
MAXXIM MEDICAL
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