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Ximed/Prosure/Injectx

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K002269ELECTROSURGICAL PROBES AND DEVICES-GELTXJanuary 4, 2001
K994151PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICESMarch 1, 2000
K983765INJECTION NEEDLE PROBE/DEVICE-TUNISDecember 11, 1998
K983200INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEXDecember 11, 1998
K981256ISOLATED SALINE ELECTRODES/PROBES/DEVICES-SALINETRODEMay 12, 1998
K974484ISOLATED ELECTROSURGICAL PROBES AND DEVICES-SALINETRODEFebruary 10, 1998
K974637ELECTRODES/PROBES/DEVICESJanuary 7, 1998
K962593ELECTROSURGICAL PROBES & DEVICESNovember 12, 1996
K945995BIPOLAR ELECTROSURGICAL PROBES AND INSTRUMENTSJanuary 31, 1995