Ad-Tech Medical Instrument Corp
Ad-Tech Medical Instrument Corp holds FDA 510(k) medical device clearances, first cleared 1985, most recent 2012.
Top product codes for Ad-Tech Medical Instrument Corp
Recent clearances by Ad-Tech Medical Instrument Corp
- K112094 — BRAIN BIOPSY NEEDLE
- K053363 — DUAL-SIDED INTERHEMISPHERIC SUBDURAL ELECTRODES, GRID SUBDURAL ELECTRODES, INTRAOPERATIVE SUBDURAL ELECTRODES
- K053358 — DEPTH ELECTRODE, FORAMEN OVALE DEPTH ELECTRODES, WYLER SPHENOIDAL DEPTH ELECTRODES
- K041604 — MACRO-MICRO DEPTH ELECTRODE
- K990788 — AD-TECH'S FORAMEN OVALE ELECTRODE
- K992194 — CORTICAL MAPPING UNIT, MODEL CMU
- K973454 — AD-TECH'S SPINAL ELECTRODE
- K964644 — AD-TECH'S DEPTH ELECTRODE
- K970587 — AD-TECH SUBDURAL ELECTRODE
- K940320 — AD-TECH'S RAAB INFANT NASOPHARYNGEAL PRONGS
- K944061 — CUEVA CRANIAL NERVE ELECTRODE
- K924348 — AD-TECH'S BRAIN BIOPSY NEEDLE FOR STEREOTAXIC
- K923803 — AD-TECH SUB DURAL ELECTRODEDS
- K912760 — AD-TECH EPIDURAL PEG ELECTRODE
- K891920 — AD-TECH'S DEPTH ELECTRODE
- K864194 — PALMER OBSTETRIC BRACE
- K861031 — WYLER SPHENOIDAL ELECTRODE
- K850342 — WYLER SUBDURAL STRIP ELECTRODE
Data sourced from openFDA. This site is unofficial and independent of the FDA.