Ad-Tech Medical Instrument Corp
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 18
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K112094 | BRAIN BIOPSY NEEDLE | April 24, 2012 |
| K053363 | DUAL-SIDED INTERHEMISPHERIC SUBDURAL ELECTRODES, GRID SUBDURAL ELECTRODES, INTRAOPERATIVE SUBDURAL E | May 30, 2006 |
| K053358 | DEPTH ELECTRODE, FORAMEN OVALE DEPTH ELECTRODES, WYLER SPHENOIDAL DEPTH ELECTRODES | May 25, 2006 |
| K041604 | MACRO-MICRO DEPTH ELECTRODE | August 16, 2004 |
| K990788 | AD-TECH'S FORAMEN OVALE ELECTRODE | November 2, 1999 |
| K992194 | CORTICAL MAPPING UNIT, MODEL CMU | September 13, 1999 |
| K973454 | AD-TECH'S SPINAL ELECTRODE | June 10, 1998 |
| K964644 | AD-TECH'S DEPTH ELECTRODE | May 9, 1997 |
| K970587 | AD-TECH SUBDURAL ELECTRODE | May 9, 1997 |
| K940320 | AD-TECH'S RAAB INFANT NASOPHARYNGEAL PRONGS | September 19, 1995 |
| K944061 | CUEVA CRANIAL NERVE ELECTRODE | January 20, 1995 |
| K924348 | AD-TECH'S BRAIN BIOPSY NEEDLE FOR STEREOTAXIC | November 23, 1992 |
| K923803 | AD-TECH SUB DURAL ELECTRODEDS | October 23, 1992 |
| K912760 | AD-TECH EPIDURAL PEG ELECTRODE | January 15, 1992 |
| K891920 | AD-TECH'S DEPTH ELECTRODE | July 27, 1989 |
| K864194 | PALMER OBSTETRIC BRACE | January 14, 1987 |
| K861031 | WYLER SPHENOIDAL ELECTRODE | August 25, 1986 |
| K850342 | WYLER SUBDURAL STRIP ELECTRODE | July 30, 1985 |