FDA 510(k) Applications Submitted by RELIANCE MEDICAL CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K012042 06/29/2001 KINETIC CANNULA RELIANCE MEDICAL CORP.
K012044 06/29/2001 BI-PHASIC INFILTRATOR RELIANCE MEDICAL CORP.


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