George King Bio-Medical, Inc. is one of 4732 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
George King Bio-Medical, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
George King Bio-Medical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Overland Park, US.
Historical record: 5 cleared submissions from 1995 to 2017. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by George King Bio-Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - George King Bio-Medical, Inc.
5 devices
Cleared
Feb 23, 2017
George King Coumadin Plasma
Hematology
288d
Cleared
Oct 24, 1995
B-FACT, BORDERLINE FACTOR ASSAY CONTROL
Hematology
344d
Cleared
Oct 24, 1995
A-FACT, ABNORMAL FACTOR ASSAY CONTROL
Hematology
344d
Cleared
Oct 20, 1995
PROTEIN C DEFICIENT PLASMA
Hematology
340d
Cleared
Oct 05, 1995
POSITIVE LUPUS ANTICOAGULANT PLASMA
Hematology
325d