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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact