Perfusion Partners & Assoc., 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 |
|---|
| K070666 | GENESISCS COMPONENT CONCENTRATING SYSTEM | June 20, 2007 |
| K024080 | SECQUIRE CELL SEPARATOR | July 2, 2003 |