Cryosan, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cryosan, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Cryosan, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1981 to 1983. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Cryosan, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cryosan, Inc.
6 devices
Cleared
Jul 19, 1983
INFUSION PUMP
Gastroenterology & Urology
34d
Cleared
Jun 16, 1983
AUTOMATED BLOOD CELL SEPARATOR
Hematology
92d
Cleared
Sep 30, 1982
AUTOMATED BLOOD CELL SEPARATOR
Hematology
38d
Cleared
Mar 04, 1982
ROCKING/CIRCULATING CYTO-THERM II 3570
Hematology
93d
Cleared
Sep 16, 1981
CRYOSAN NORMAL SALINE
Chemistry
30d
Cleared
Sep 16, 1981
CIRCULATING CYTO-THERMS
Hematology
30d