Hyclone Laboratories, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Hyclone Laboratories, Inc. has 11 FDA 510(k) cleared pathology devices. Based in Logan, US.
Historical record: 11 cleared submissions from 1987 to 1988.
Browse the complete list of FDA 510(k) cleared pathology devices from this manufacturer. Filter by specialty or product code using the sidebar.
11 devices
Cleared
Nov 30, 1988
ALPHACALF SERUM
Pathology
23d
Cleared
Apr 04, 1988
BOVINE CALF SERUM SUPPLEMENTED #A-2159
Pathology
61d
Cleared
Apr 01, 1988
BOVINE CALF SERUM CATALOG #A-2119
Pathology
58d
Cleared
Mar 31, 1987
FETAL BOVINE SERUM
Pathology
22d
Cleared
Mar 24, 1987
DEFINED FETAL BOVINE SERUM #A-1111
Pathology
49d
Cleared
Mar 24, 1987
CHARACTERIZED FETAL BOVINE SERUM #A-1115
Pathology
49d
Cleared
Mar 24, 1987
6/40 FETAL BOVINE SERUM #A-1110
Pathology
49d
Cleared
Mar 24, 1987
DEFINED CALF BOVINE SERUM #A-2111
Pathology
49d
Cleared
Mar 24, 1987
DEFINED CALF BOVINE SERUM SUPPLEMENTED #A-2151
Pathology
49d
Cleared
Mar 24, 1987
ADULT BOVINE SERUM
Pathology
49d
Cleared
Mar 24, 1987
DEFINED EQUINE SERUM #A-3311
Pathology
49d