Burroughs Wellcome Co. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Burroughs Wellcome Co. has 17 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 17 cleared submissions from 1977 to 1982.
Browse the FDA 510(k) cleared devices submitted by Burroughs Wellcome Co. Filter by specialty or product code using the sidebar.
17 devices
Cleared
Feb 18, 1982
WELLCOGEN GROUP B
Microbiology
37d
Cleared
Dec 29, 1981
SAC-CEL
Pathology
14d
Cleared
Apr 17, 1981
DAC-CEL HCG
Chemistry
80d
Cleared
Mar 06, 1981
DAC-CEL DIAGNATAL
Chemistry
38d
Cleared
Feb 10, 1981
DAC-CEL T3 UPTAKE
Chemistry
14d
Cleared
Feb 10, 1981
DAC-CEL TSH
Chemistry
14d
Cleared
Sep 04, 1979
DAC-CEL T4
Chemistry
64d
Cleared
Sep 04, 1979
DAC-CEL T3
Chemistry
64d
Cleared
Oct 17, 1978
STREP-TEX
Immunology
29d
Cleared
Jun 14, 1978
THYMUNE-M
Immunology
15d
Cleared
Jun 14, 1978
THYMUNE-T
Immunology
15d
Cleared
Apr 24, 1978
DAC-CEL DIGOXIN RADIOIMMUNOASSAY KIT
Toxicology
31d
Cleared
Sep 15, 1977
TOXHA TEST
Toxicology
31d
Cleared
Sep 02, 1977
FLUORESCENT ANTI. ANTI-HUMAN C3
Microbiology
15d
Cleared
Aug 25, 1977
AGGLUTINATING SERUM W135
Immunology
10d
Cleared
Jul 14, 1977
CRP-WELLCOTEST
Immunology
17d
Cleared
Mar 16, 1977
CAMMADISK DIGOXIN
Toxicology
33d