Kallestad Diag, A Div. of Erbamont, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kallestad Diag, A Div. of Erbamont, Inc. - FDA 510(k) Cleared Devices
58
Total
58
Cleared
0
Denied
Kallestad Diag, A Div. of Erbamont, Inc. has 58 FDA 510(k) cleared medical devices. Based in Chaska, US.
Historical record: 58 cleared submissions from 1987 to 1991. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Kallestad Diag, A Div. of Erbamont, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kallestad Diag, A Div. of Erbamont, Inc.
58 devices
Cleared
Jun 17, 1991
QM300 CALIBRATOR G PACK
Microbiology
105d
Cleared
Jun 17, 1991
QM300 ANTISTREPTOLYSIN O (ASO) ANTIGEN PACK
Microbiology
105d
Cleared
Jun 17, 1991
QM300 CONTROL G PACK
Microbiology
105d
Cleared
Jan 14, 1991
CHLAMYDIA SYSTEM SOFTWARE (CSS)
Microbiology
89d
Cleared
Jul 26, 1990
PATHFINDER(TM) CHLAMYDIA MICROPLATE KIT
Microbiology
66d
Cleared
Jun 21, 1990
MODIFIED QM300 RHEUMATOID FACTOR TEST
Immunology
17d
Cleared
Apr 03, 1990
NDS CORTISOL TEST KIT AND NDS CORTISOL CALIBRATOR
Toxicology
91d
Cleared
Mar 29, 1990
NDS THYROXINE TEST KIT & NDS THYROXINE CALIBRATOR
Chemistry
97d
Cleared
Mar 29, 1990
NDS THEOPHYLLINE TEST KIT & NDS TDM CALIBRATOR SET
Toxicology
86d
Cleared
Mar 23, 1990
PLATELIA TOXO IGG KIT
Microbiology
232d
Cleared
Mar 15, 1990
PLATELIA TOXO IGM KIT
Microbiology
224d
Cleared
Jan 22, 1990
ALLERCOAT MICROPLATE SYSTEM
Immunology
19d
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