Diagnostic Specialties is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diagnostic Specialties - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Diagnostic Specialties has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1981 to 1997. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Diagnostic Specialties Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Diagnostic Specialties
8 devices
Cleared
Sep 02, 1997
ENZIP IMMUNOTURBIDIMETRIC MICROALBUMIN ASSAY KIT
Chemistry
133d
Cleared
Aug 30, 1994
ENZIP IMMUNOTURBIDMETRIC FIBRINOGEN ASSAY KIT
Hematology
182d
Cleared
Aug 19, 1993
PROTEIN-BOUND GLUCOSE ASSAYN KIT
Hematology
183d
Cleared
Jul 30, 1992
ENZIP URINARY MICROALBUMIN TEST
Chemistry
90d
Cleared
May 27, 1983
PREGNA-CERT, SLIDE PREGNANCY TEST
Chemistry
46d
Cleared
Nov 10, 1982
GENERIC PREGNANCY TEST
Chemistry
20d
Cleared
Jan 22, 1982
POTASSIUM REAGENT SET
Chemistry
24d
Cleared
Dec 31, 1981
GLUCOSE ENZYME-COLOR REAGENT SET
Chemistry
27d