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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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