Ventrex Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ventrex Laboratories, Inc. - FDA 510(k) Cleared Devices
82
Total
82
Cleared
0
Denied
Ventrex Laboratories, Inc. has 82 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 82 cleared submissions from 1979 to 1992. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Ventrex Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ventrex Laboratories, Inc.
82 devices
Cleared
Mar 13, 1992
SPECIFIC IGE EIA-TURBO ASSAY
Immunology
154d
Cleared
Feb 21, 1992
VENTREX ALLERGEN DISC
Immunology
179d
Cleared
Oct 25, 1991
VENTREX COATED TUBE INTACT PTH
Chemistry
85d
Cleared
Feb 21, 1991
VENTREX COATED TUBE IGE RADIOIMMUNOASSAY
Immunology
69d
Cleared
Feb 07, 1991
VENTREX COATED TUBE IGE ENZYME IMMUNOASSAY
Immunology
52d
Cleared
Jan 17, 1991
SHBG IRMA KIT
Chemistry
57d
Cleared
Dec 07, 1990
TURBO-RAST SPECIFIC IGE ASSAY
Immunology
78d
Cleared
Jul 31, 1990
TURBO-RAST SPECIFIC IGE ASSAY
Immunology
22d
Cleared
Jan 22, 1990
VENTRESIGN STREP A TEST
Microbiology
33d
Cleared
Jan 18, 1990
COATED TUBE HIGH SENSITIVITY TSH 100 UIU/ML STAN.
Chemistry
120d
Cleared
Jan 18, 1990
COATED TUBE HIGH SENSITIVITY TSH 200 UIU/ML STAN.
Chemistry
120d
Cleared
Dec 18, 1989
VENTREX COATED TUBE IGE ENZYME IMMUNOASSAY
Immunology
13d
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