Louisville Apl Diagnostics, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K021398 | APL IGA ELISA KIT | August 27, 2002 |
| K984102 | ACL/APS FACS KIT | March 18, 1999 |
| K933588 | APHLELISA KIT | October 13, 1994 |