Izon Business Products, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K010328 | MULTIPLE (IZON DNA BLOOD COLLECTION KIT) | April 9, 2001 |
| K950257 | MULTIPLE (IZON DBS & URINE COLLECTION KIT) | April 14, 1995 |
| K950246 | MULTIPLE (IZON URINE COLLECTION KIT) | March 21, 1995 |
| K950221 | MULTIPLE (IZON BLOOD & URINE COLLECTION KIT) | March 21, 1995 |