Dilon Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K110384 | DILON 6800 ACELLA (ACELLA) | May 3, 2011 |
| K082588 | GAMMALOC SYSTEM, MODEL 03-00001 | December 11, 2009 |
| K984466 | DILON 2000, MODEL 2000-6X8 AND DILON 2000, MODEL 2000-5X5 | March 16, 1999 |