Medical Engineering and Development Institute
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K902477 | WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL SET | August 24, 1990 |
| K902469 | BYRD DILATOR SHEATH SET - TEFLON | August 23, 1990 |
| K902502 | BYRD STAINLESS STEEL DILATOR | August 7, 1990 |
| K895030 | LIFE-LINE(TM) VASCULAR ACCESS SYSTEM | April 17, 1990 |
| K893480 | BYRD EXTRACTOR SET | June 23, 1989 |
| K890820 | LOCKING WIRE GUIDE STYLET | March 22, 1989 |