Neuro-Diagnostic Assoc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K980866 | MEDI-DX 7000 CPT WITH AMREX ELECTRODES | May 20, 1998 |
| K964622 | MEDI-DX 7000 | December 1, 1997 |