General Diagnostics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
General Diagnostics - FDA 510(k) Cleared Devices
39
Total
39
Cleared
0
Denied
General Diagnostics has 39 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 39 cleared submissions from 1976 to 1988.
Browse the FDA 510(k) cleared devices submitted by General Diagnostics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - General Diagnostics
39 devices
Cleared
Sep 19, 1988
BARBITURATE ENZYME IMMUNOASSAY KIT
Toxicology
84d
Cleared
Nov 03, 1987
CANNABINOID ENZYME IMMUNOASSAY KIT
Toxicology
104d
Cleared
Jun 05, 1987
COCAINE METABOLITE ENZYME IMMUNOASSAY KIT
Toxicology
65d
Cleared
Mar 31, 1987
QUALI. ENZYME IMMUNO. OF BARBITURATES IN URINE
Toxicology
99d
Cleared
Mar 12, 1987
BENZODIAZEPINE ENZYME IMMUNOASSAY KIT
Toxicology
157d
Cleared
Jul 20, 1984
GENERAL DIAG. CEFONICID 30MCG ANTIMIC
Microbiology
38d
Cleared
Jul 02, 1984
GENERAL DIAGNOSTICS PLATELET ANTIBODY
Immunology
84d
Cleared
Dec 30, 1983
CEFTIZOXIME 30 MCG ANTIMICROBIAL DISK
Microbiology
71d
Cleared
Oct 14, 1983
CEFUROXIME 30MCG. SUSCEP DISK
Microbiology
67d
Cleared
May 09, 1983
CEFAZOLIN 30MCG. ANTIMICROBIAL SUSCEP
Microbiology
28d
Cleared
Apr 08, 1983
NETILMICIN 30 MCG ANTIMICROBIAL DISK
Microbiology
31d
Cleared
Jan 21, 1983
VON WILLEBRAND FACTOR ASSAY
Hematology
65d
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