Vee Gee Scientific, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K941901 | MODEL 2721 CLINICAL REFRACTOMETER | January 17, 1995 |
| K941903 | MODEL 2740 CLINICAL REFRACTOMETER | January 17, 1995 |
| K941906 | MODEL 2730 CLINICAL REFRACTOMETER | January 17, 1995 |
| K941902 | MODEL 3471 CLINICAL REFRACTOMETER | December 13, 1994 |
| K941905 | MODEL 3461 CLINICAL REFRACTOMETER | December 13, 1994 |
| K941904 | MODEL A300CL CLINICAL REFRACTOMETER | December 13, 1994 |