London Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
London Diagnostics, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
London Diagnostics, Inc. has 12 FDA 510(k) cleared chemistry devices. Based in Eden Prairie, US.
Historical record: 12 cleared submissions from 1988 to 1991.
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 - London Diagnostics, Inc.
12 devices
Cleared
Dec 17, 1991
LUMATAG FREE T4 CHEMILUMINESCENCE ASSAY
Chemistry
53d
Cleared
Aug 02, 1991
LUMATAG T4 CHEMILUMINESCENCE ASSAY
Chemistry
88d
Cleared
Jul 30, 1991
LONDON DIAGNOSTICS LUMATAG(R) HGH CHEM IMMUN ASSAY
Chemistry
32d
Cleared
Feb 04, 1991
LUMATAG(R) FSH CHEMILUMINESCENCE IMMUNOMETRI ASSAY
Chemistry
38d
Cleared
Oct 12, 1990
LUMATAG(TM) PROLACTIN DIAGNOSTIC KIT/MODIFICATION
Chemistry
11d
Cleared
Sep 25, 1990
LONDON DIAGNOSTICS LUMATAG(TM) INTACT PTH ASSAY
Chemistry
70d
Cleared
Aug 02, 1990
LUMATAG(TM) LH DIAGNOSTIC KIT
Chemistry
62d
Cleared
Aug 02, 1990
LONDON DIAGNOSTICS LUMATAG (R) IGE CHEM. IMM ASSAY
Immunology
14d
Cleared
May 01, 1990
LUMATAG(TM) HCG CHEMILUMINESCENCE IMMUNOMETRIC
Chemistry
33d
Cleared
Apr 02, 1990
LUMATAG(TM) FERRITIN CHEMILUMINESCENCE IMMUNOMET.
Immunology
25d
Cleared
May 27, 1988
LUMATAG(TM) TSH CHEMILUMINESCENCE IMMUNO. ASSAY
Chemistry
52d
Cleared
Mar 24, 1988
LUMATAG(TM) PROLACTIN CHEMILUMINES. IMMUNO. ASSAY
Chemistry
59d