Cryosan, Inc.
Cryosan, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 19, 1983.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K831953 | INFUSION PUMP | July 19, 1983 |
| K830831 | AUTOMATED BLOOD CELL SEPARATOR | June 16, 1983 |
| K822521 | AUTOMATED BLOOD CELL SEPARATOR | September 30, 1982 |
| K813489 | ROCKING/CIRCULATING CYTO-THERM II 3570 | March 4, 1982 |
| K812311 | CIRCULATING CYTO-THERMS | September 16, 1981 |
| K812309 | CRYOSAN NORMAL SALINE | September 16, 1981 |