Kallestad Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kallestad Laboratories, Inc. - FDA 510(k) Cleared Devices
92
Total
92
Cleared
0
Denied
Kallestad Laboratories, Inc. has 92 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 92 cleared submissions from 1976 to 1986. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Kallestad Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kallestad Laboratories, Inc.
92 devices
Cleared
Dec 03, 1986
PATHFINDER(TM) DIRECT ANTIGEN DETECTION SYSTEM
Microbiology
75d
Cleared
Oct 22, 1986
PATHFINDER ROTAVIRUS CHEMILUMINESCENT
Microbiology
82d
Cleared
Oct 10, 1986
PATHFINDER(TM) SPECIMEN COLLECTION KIT
Microbiology
21d
Cleared
Sep 29, 1986
PATHFINDER(TM) RESPIRATORY SYNCYTIAL VIRUS
Microbiology
70d
Cleared
Aug 06, 1986
KALLESTAD SM/RNP TEST REAGENT
Immunology
49d
Cleared
Jul 29, 1986
KALLESTAD SSA/SSB ENA TEST REAGENTS
Immunology
13d
Cleared
Mar 14, 1986
QUANTIMETRIC PLUS CALIBRATOR/CONTROL SET A
Immunology
88d
Cleared
Feb 28, 1986
QUANTIMETRIC PLUS IGM REAGENT KIT
Immunology
74d
Cleared
Feb 26, 1986
QUANTIMETRIC PLUS LAMBDA REAGENT KIT
Immunology
72d
Cleared
Feb 26, 1986
QUANTIMETRIC PLUS KAPPA REAGENT KIT
Immunology
72d
Cleared
Feb 26, 1986
QUANTIMETRIC PLUS IGA REAGENT KIT
Immunology
72d
Cleared
Feb 26, 1986
QUANTIMETRIC PLUS C3 REAGENT KIT
Immunology
72d
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