Mid-Atlantic Diagnostics, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K100596 | CRYOPETTE | December 6, 2010 |
| K041435 | THE STRIPPER PGD | September 29, 2004 |
| K030525 | CUSTOM PRODUCTS IVF WORKSTATION TYPE WKST-24*36, WKST-24*48, WKST-24*60, WKST-24*72 AND WKST-24*72D | August 27, 2003 |
| K993699 | THE STRIPPER | May 16, 2000 |