Novo Nordisk Diagnostics, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K911430 | IDEIA(TM) CHLAMYDIA, MODIFICATION | August 7, 1991 |
| K901972 | ADD'L CLAIMED INTENDED USE FOR IDEIA(TM) CHLAMYDIA | September 5, 1990 |