Cryosan, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K831953INFUSION PUMPJuly 19, 1983
K830831AUTOMATED BLOOD CELL SEPARATORJune 16, 1983
K822521AUTOMATED BLOOD CELL SEPARATORSeptember 30, 1982
K813489ROCKING/CIRCULATING CYTO-THERM II 3570March 4, 1982
K812311CIRCULATING CYTO-THERMSSeptember 16, 1981
K812309CRYOSAN NORMAL SALINESeptember 16, 1981