FDA 510(k) Applications Submitted by UROMED CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K010098 01/11/2001 MODIFICATION TO CAVERMAP SURGICAL AID UROMED CORP.
K010213 01/23/2001 MODIFICATION TO CAVERMAP SURGICAL AID UROMED CORP.
K000507 02/15/2000 CAVERMAP SURGICAL AID UROMED CORP.
K970971 03/17/1997 URO MED NERVE STIMULATOR UROMED CORP.
K982226 06/24/1998 UROMED BRACHYTHERAPHY IODINE-125 SOURCES UROMED CORP.
K993436 10/12/1999 CAVERMAP SURGICAL AID UROMED CORP.
K974137 11/03/1997 UROMED NEEDLE GRASPER UROMED CORP.
K974600 12/09/1997 UROMED PATCH UROMED CORP.
K980717 02/24/1998 UROMED SLING KIT UROMED CORP.
K971992 05/29/1997 UROMED ALTERNATIVE BLADDER CONTROL CONTINENCE DEVICE(ABCPN-0026) UROMED CORP.


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