FDA 510(k) Applications Submitted by MARY WILEN

FDA 510(k) Number Submission Date Device Name Applicant
K970704 02/26/1997 PERSONAL CATHETER ROCHESTER MEDICAL CORP.
K000723 03/06/2000 HYDROPHILIC SILICONE FOLEY CATHETER AND PERSONAL CATHETER (HYDROPHILIC AND NON-HYDROPHILIC) ROCHESTER MEDICAL CORP.
K001143 04/10/2000 RELEASE NF ANTIBACTERIAL FOLEY CATHETER, ANTIBACTERIAL PERSONAL CATHETER ROCHESTER MEDICAL CORP.
K981612 05/06/1998 ALL SILICONE FOLEY CATHETER, TWO-WAY FOLEY CATHETER, THREE-WAY FOLEY CATHETER, TWO-WAY RADIOPAQUE FOLEY CATHETER ROCHESTER MEDICAL CORP.


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