FDA 510(k) Applications Submitted by AD-TECH MEDICAL INSTRUMENT CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K973454	09/11/1997	AD-TECH'S SPINAL ELECTRODE	AD-TECH MEDICAL INSTRUMENT CORP.
K970587	02/18/1997	AD-TECH SUBDURAL ELECTRODE	AD-TECH MEDICAL INSTRUMENT CORP.
K990788	03/10/1999	AD-TECH'S FORAMEN OVALE ELECTRODE	AD-TECH MEDICAL INSTRUMENT CORP.
K964644	10/31/1996	AD-TECH'S DEPTH ELECTRODE	AD-TECH MEDICAL INSTRUMENT CORP.
K041604	06/14/2004	MACRO-MICRO DEPTH ELECTRODE	AD-TECH MEDICAL INSTRUMENT CORP.
K053358	12/02/2005	DEPTH ELECTRODE, FORAMEN OVALE DEPTH ELECTRODES, WYLER SPHENOIDAL DEPTH ELECTRODES	AD-TECH MEDICAL INSTRUMENT CORP.
K053363	12/02/2005	DUAL-SIDED INTERHEMISPHERIC SUBDURAL ELECTRODES, GRID SUBDURAL ELECTRODES, INTRAOPERATIVE SUBDURAL ELECTRODES	AD-TECH MEDICAL INSTRUMENT CORP.
K112094	07/22/2011	BRAIN BIOPSY NEEDLE	AD-TECH MEDICAL INSTRUMENT CORP.
K992194	06/29/1999	CORTICAL MAPPING UNIT, MODEL CMU	AD-TECH MEDICAL INSTRUMENT CORP.