Biodiagnostic Intl is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biodiagnostic Intl - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Biodiagnostic Intl has 11 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1983 to 2004. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Biodiagnostic Intl Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biodiagnostic Intl
11 devices
Cleared
Oct 15, 2004
LIQUI-HEME GLYCO A1C ASSAY
Chemistry
541d
Cleared
Jul 08, 1988
LIQUI-SERA SERUM ALCOHOL CONTROLS
Toxicology
94d
Cleared
Dec 29, 1987
LIQUI-SERA SPINAL FLUID CONTROL
Chemistry
61d
Cleared
Nov 24, 1986
LIQUI-SERA COMBO LIGAND/TDM CONTROLS
Chemistry
55d
Cleared
Oct 04, 1985
LIQUI-SERA CHEMISTRY CONTROLS (COMPREHENSIVE)
Chemistry
14d
Cleared
Sep 30, 1985
LIQUI-SERA CHEM. MULTIPLE CALIBRATORS
Chemistry
11d
Cleared
Mar 05, 1985
LIQUI-HEME HEMOGLOBIN CALIBRATORS
Chemistry
238d
Cleared
Apr 04, 1984
LIQUI-URA CHEMISTRY URINE CONTROLS
Chemistry
50d
Cleared
Feb 03, 1984
LIQUI-SERA TDM CALIBRATORS
Toxicology
51d
Cleared
Jan 30, 1984
LIQUI-URA TOXIC URINE CONTROL
Toxicology
54d
Cleared
May 27, 1983
LIQUI-SERA ANTICONVULSANTS CONTROLS
Toxicology
38d