Geometric Data, Div. Smithkline Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Geometric Data, Div. Smithkline Corp. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Geometric Data, Div. Smithkline Corp. has 18 FDA 510(k) cleared hematology devices. Based in Mchenry, US.
Historical record: 18 cleared submissions from 1976 to 1984.
Browse the complete list of FDA 510(k) cleared hematology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Geometric Data, Div. Smithkline Corp.
18 devices
Cleared
Sep 05, 1984
AUTOLYZER 800
Hematology
125d
Cleared
Aug 18, 1981
HEMASPINNER
Hematology
78d
Cleared
Sep 04, 1979
HEMATRAK ABNORMAL RECOGNITION
Hematology
91d
Cleared
Jul 17, 1979
HEMATRAK MODEL 480
Hematology
81d
Cleared
Jul 17, 1979
CONTEXT FILTER
Hematology
33d
Cleared
Feb 15, 1979
STAIN, HEMASTAIN RETIC
Hematology
41d
Cleared
May 19, 1978
PLATELETS/CU MM
Hematology
39d
Cleared
Jan 05, 1978
RE-CELL SLIDE RECAP
Hematology
52d
Cleared
Oct 18, 1977
HEMATRAK RBC MORPHOLOGY
Hematology
315d
Cleared
Jul 01, 1977
HEMATRAK
Hematology
81d
Cleared
Jun 17, 1977
ATYPIA PROFILE MONITOR
Hematology
88d
Cleared
Jun 03, 1977
HEMATRAK MODEL 125
Hematology
46d