Kent Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kent Laboratories, Inc. - FDA 510(k) Cleared Devices
40
Total
37
Cleared
0
Denied
Kent Laboratories, Inc. has 37 FDA 510(k) cleared immunology devices. Based in Mchenry, US.
Historical record: 37 cleared submissions from 1977 to 1995.
Browse the complete list of FDA 510(k) cleared immunology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kent Laboratories, Inc.
40 devices
Cleared
Jun 01, 1995
HUMAN PREALBUMIN RADIAL IMMUNODIFFUSION KIT
Immunology
35d
Cleared
May 30, 1995
HUMAN C1 INACTIVATOR OR C-1 ESTERASE INHIBITOR RADIAL IMMUNODIFFUSION KIT
Immunology
33d
Cleared
May 30, 1995
HUMAN C1Q RADIAL IMMUNODIFFUSION KIT
Immunology
33d
Cleared
Apr 10, 1995
HUMAN C-5 RADIAL IMMUNODIFFUSION KIT
Immunology
89d
Cleared
Nov 27, 1985
72 DETERM. SIZE RADIAL IMMUNODIFFUSION TEST ALPHA2
Immunology
279d
Cleared
Nov 25, 1985
72 DETERM. SIZE RADIAL IMMUNO. TEST HUMAN CERULOPL
Immunology
277d
Cleared
Nov 01, 1985
ANTISERUM TO HUMAN PREALBUMIN
Immunology
253d
Cleared
Nov 01, 1985
ANTISERUM TO HUMAN APOLIPOPROTEIN B
Immunology
253d
Cleared
Nov 01, 1985
ANTISERUM TO HUMAN APOLIPOPROTEIN A-I
Immunology
253d
Cleared
Aug 11, 1983
IMMUNODIFFUSION TEST HUMAN ANTITHROMBIN
Chemistry
55d
Cleared
Jul 19, 1983
RADIAL IMMUNO-TEST FOR HUMAN C-REACTI
Chemistry
32d
Cleared
Jul 19, 1983
RADIAL IMMUNO-TEST FOR HUMAN FACTOR B
Chemistry
32d
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