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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.
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