Allelix 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 |
|---|
| K885298 | VISUWELL REAGIN TEST 960 TEST KIT | March 15, 1989 |
| K880665 | MODIFIED GROUP A STREPTOCOCCUS DETECTION KIT | March 1, 1988 |