Equal Diagnostics, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K981800 | SENTINEL CHOLINESTERASE LIQUID MODEL NUMBER 17.019A & 17.606 | July 6, 1998 |
| K961179 | SENTINEL LIPASE LIQUID MODEL 17.401B | July 19, 1996 |