Leeco Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Leeco Diagnostics, Inc. - FDA 510(k) Cleared Devices
49
Total
49
Cleared
0
Denied
Leeco Diagnostics, Inc. has 49 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.
Historical record: 49 cleared submissions from 1979 to 1989.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Leeco Diagnostics, Inc.
49 devices
Cleared
Oct 31, 1989
LEECO PREVIEW(R) EBV (EIA)
Immunology
35d
Cleared
Aug 15, 1989
LEECO VIS-DISK STREP-A (EIA)
Microbiology
64d
Cleared
Jun 16, 1989
VIS-DISK HCG (EIA) LYOPHILIZED JPL-044M
Chemistry
106d
Cleared
Jun 16, 1989
VIS-DISK HCG (EIA) JPL-041M
Chemistry
106d
Cleared
Sep 13, 1988
PRL-QUANT
Chemistry
41d
Cleared
Mar 15, 1988
CONCEP-7-BHCG
Chemistry
34d
Cleared
Feb 11, 1988
LEECO PREGNASTICK (EIA) CATALOG #003
Chemistry
31d
Cleared
Mar 10, 1987
VIS-CUBE HCG (EIA) LYOPHILIZED JPL-044
Chemistry
46d
Cleared
Feb 03, 1987
LEECO VIS-CUBE STREP A (EIA)
Microbiology
102d
Cleared
Jan 09, 1987
VIS-CUBE PREGNANCY HOME TEST,CAT. # JPL-042
Chemistry
87d
Cleared
Dec 15, 1986
VIS-CUBE HCG (EIA)
Chemistry
68d
Cleared
Sep 16, 1986
RIGHT-DAY OVULATION HOME TEST
Chemistry
159d
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