Damon Corp. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Damon Corp. has 11 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1976 to 1987. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Damon Corp. Filter by specialty or product code using the sidebar.
11 devices
Cleared
Dec 23, 1987
DAMON D.E.T.E.C.T IMAGE ENHANCER
Radiology
26d
Cleared
Jul 18, 1983
ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY
Microbiology
41d
Cleared
Apr 01, 1982
LIQUISOL PROGESTERONE RADIOIMMUNO
Chemistry
21d
Cleared
Dec 10, 1980
LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT
Chemistry
43d
Cleared
Apr 04, 1979
LIQUISOL CORTISOL RIA TEST KIT
Toxicology
57d
Cleared
Feb 26, 1979
IEC CENTRA-7 CENTRIFUGE MODEL 2362
Chemistry
61d
Cleared
Jul 27, 1978
RIA TEST KIT SYS. DAMON KIQUISOL FREE
Hematology
41d
Cleared
Feb 23, 1978
LIQUISOL DIGOXIN RIA TEST KIT
Toxicology
16d
Cleared
Jun 17, 1977
LIQUI SOL T4 RIA TEST KIT
Chemistry
29d
Cleared
May 06, 1977
ANALYZEO, PLASMA, BLOOD, COLYSAGRAPH
Hematology
36d
Cleared
Nov 16, 1976
SPINETTE CENTRIFUGE
Chemistry
7d