Connecticut Diagnostics, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Connecticut Diagnostics, Ltd. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Connecticut Diagnostics, Ltd. has 14 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1979 to 1991.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Connecticut Diagnostics, Ltd.
14 devices
Cleared
Mar 29, 1991
VISI-STAPH
Microbiology
105d
Cleared
Sep 17, 1982
CDL LYSING REAGENT
Hematology
30d
Cleared
Sep 17, 1982
CDL ISOTONIC DILUENT
Hematology
30d
Cleared
Sep 17, 1982
CDL AUTO-LYSING REAGENT
Hematology
29d
Cleared
May 21, 1981
INORGANIC PHOSPHORUS REAGENTS
Chemistry
17d
Cleared
Oct 10, 1980
GLUCOSE DIAGNOSTIC REAGENT
Chemistry
63d
Cleared
Oct 10, 1980
URIC ACID DIAGNOSTIC REAGENT
Chemistry
63d
Cleared
Dec 18, 1979
CONNECTICUT DIAGNOSTICS, LTS. DIRECT
Chemistry
15d
Cleared
Dec 06, 1979
DONNECT. DIAG. CALCIUM DIAG. REAGENT
Chemistry
17d
Cleared
Dec 06, 1979
DONNECT. DIAG. TOTAL BILIRUBIN REAGENTS
Chemistry
17d
Cleared
Dec 06, 1979
CONNECT. DIAG. ALBUMIN DIAGNOSTIC REAGEN
Chemistry
17d
Cleared
Dec 06, 1979
CONNECT. DIAG. TOTAL PROTEIN DIAG. REAGE
Chemistry
17d
Cleared
Dec 06, 1979
BLOOD UREA NITROGEN REAGENT
Chemistry
15d
Cleared
Oct 17, 1979
CREATININE DIAG. REAGENT PICRIC ACID
Chemistry
14d