Hematology Marketing Assoc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Hematology Marketing Assoc. has 14 FDA 510(k) cleared hematology devices. Based in Walker, US.
Historical record: 14 cleared submissions from 1983 to 1985.
Browse the complete list of FDA 510(k) cleared hematology devices from this manufacturer. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Jul 30, 1985
OSMOCEL 3
Hematology
95d
Cleared
Jul 12, 1985
TRI-COUNT
Hematology
95d
Cleared
Mar 29, 1985
LASER-GLOBIN POWDER
Hematology
77d
Cleared
Mar 29, 1985
LASER-DIL
Hematology
77d
Cleared
Mar 29, 1985
LASER-GLOBIN
Hematology
77d
Cleared
Mar 29, 1985
LASER-LYSE
Hematology
77d
Cleared
Mar 05, 1985
TRI-COUNT CALIBRATOR
Hematology
92d
Cleared
Dec 12, 1984
TRI-COUNT LASER
Hematology
97d
Cleared
Mar 09, 1984
TRI-COUNT 10
Hematology
87d
Cleared
Oct 20, 1983
TRI-COUNT 7
Hematology
37d
Cleared
Jun 16, 1983
HEMACAL
Hematology
55d
Cleared
Mar 01, 1983
FOCUS FLUID
Hematology
41d