Marvic Interpharma, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K854223 | VES-TEC/VES-MATIC | April 4, 1986 |
| K854222 | DIESSE RF TEST KIT | February 6, 1986 |
| K854221 | DIESSE CRP TEST KIT | November 25, 1985 |