FDA 510(k) Applications Submitted by XIMED/PROSURE/INJECTX

FDA 510(k) Number Submission Date Device Name Applicant
K981256 04/02/1998 ISOLATED SALINE ELECTRODES/PROBES/DEVICES-SALINETRODE XIMED/PROSURE/INJECTX
K962593 07/02/1996 ELECTROSURGICAL PROBES & DEVICES XIMED/PROSURE/INJECTX
K002269 07/26/2000 ELECTROSURGICAL PROBES AND DEVICES-GELTX XIMED/PROSURE/INJECTX
K983200 09/14/1998 INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEX XIMED/PROSURE/INJECTX
K945995 10/06/1994 BIPOLAR ELECTROSURGICAL PROBES AND INSTRUMENTS XIMED/PROSURE/INJECTX
K983765 10/26/1998 INJECTION NEEDLE PROBE/DEVICE-TUNIS XIMED/PROSURE/INJECTX
K974484 11/26/1997 ISOLATED ELECTROSURGICAL PROBES AND DEVICES-SALINETRODE XIMED/PROSURE/INJECTX
K974637 12/12/1997 ELECTRODES/PROBES/DEVICES XIMED/PROSURE/INJECTX
K994151 12/09/1999 PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES XIMED/PROSURE/INJECTX


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