Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by ROCHESTER MEDICAL CORP.
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.
K971627
05/02/1997
SILICONE ANTIBACTERIAL FOLEY CATHETER
ROCHESTER MEDICAL CORP.
K122785
09/11/2012
HYDROSIL; MAGIC; PERSONAL CATHETER
ROCHESTER MEDICAL CORP.
K033477
11/03/2003
HYDROPHILIC-ANTIBACTERIAL INTERMITTENT CATHETER, INTERMITTENT CATHETER CLOSED SYSTEM KIT
ROCHESTER MEDICAL CORP.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact