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Uromed Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K010213MODIFICATION TO CAVERMAP SURGICAL AIDApril 20, 2001
K010098MODIFICATION TO CAVERMAP SURGICAL AIDFebruary 1, 2001
K000507CAVERMAP SURGICAL AIDApril 21, 2000
K993436CAVERMAP SURGICAL AIDFebruary 11, 2000
K982226UROMED BRACHYTHERAPHY IODINE-125 SOURCESMay 13, 1999
K980717UROMED SLING KITMay 22, 1998
K974600UROMED PATCHMarch 31, 1998
K974137UROMED NEEDLE GRASPERJanuary 30, 1998
K970971URO MED NERVE STIMULATOROctober 27, 1997
K971992UROMED ALTERNATIVE BLADDER CONTROL CONTINENCE DEVICE(ABCPN-0026)August 1, 1997