FDA 510(k) Applications Submitted by THOMAS R GUNERMAN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K990949	03/22/1999	CLEAR-GUARD II, CLEAR-THERM HMEF, CLEAR-THERM HMEF W/ FLEXTUBE, CLEAR GUARD 11 W/ GAS MONITORING PORT	INTERSURGICAL, INC.
K983610	10/14/1998	CLEAR-GUARD MIDI, CLEAR-GUARD MIDI W/FLEXTUBE, CLEAR-THERM MINI, CLEAR-THERM MINI W/FLEXTUBE, MODELS 1644,1644-T,1831,18	INTERSURGICAL, INC.
K984481	12/16/1998	EXHALATION VALVE	INTERSURGICAL, INC.
K024270	12/23/2002	CLEAR-THERM 3 HMEF, CLEAR-THERM 3 WITH SUPERSET CATHETER MOUNT,CLEAR-THERM WITH FLEXIBLE CATHETER MOUNT,CLEAR-GUARD 3 F3	INTERSURGICAL, INC.