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FDA 510(k) Applications Submitted by LUIS CANDELARIO
FDA 510(k) Number
Submission Date
Device Name
Applicant
K960051
01/04/1996
NIPRO SAFELET CATH
NISSHO CORP.
K955182
11/13/1995
NIPRO ARTERIAL VENOUS FISTULA NEEDLE
NISSHO CORP.
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