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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.
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