FDA 510(k) Applications Submitted by MICHAEL KWAN, PH.D.

FDA 510(k) Number Submission Date Device Name Applicant
K972358 06/25/1997 ORATEC MODEL ENDOTAC PROBE ORATEC INTERVENTIONS, INC.
K973158 08/22/1997 ORATEC INTERVENTIONS MODEL ORASTAT MONOPOLAR CAUTERY DEVICE ORATEC INTERVENTIONS, INC.
K973159 08/22/1997 ORATEC INTERVENTIONS MODEL ORA 40 ELECTROTHERMAL GENERATOR ORATEC INTERVENTIONS, INC.
K974464 11/26/1997 ORATEC SPINECATH INTRADISCAL CATHETER ORATEC INTERVENTIONS, INC.
K965007 12/16/1996 ORATEC INTERVENTIOUNS ELECTROSURGICAL PROBES ORATEC INTERVENTIONS, INC.


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