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
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