Fairleigh Dickinson Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fairleigh Dickinson Laboratories, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Fairleigh Dickinson Laboratories, Inc. has 7 FDA 510(k) cleared medical devices. Based in Allendale, US.
Historical record: 7 cleared submissions from 1985 to 1990. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Fairleigh Dickinson Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Fairleigh Dickinson Laboratories, Inc.
7 devices
Cleared
Jan 29, 1990
MODIFIED ELISA FOR CHLAMYDIA
Chemistry
105d
Cleared
Oct 24, 1989
FDL, INC.'S TRANSPORT SYSTEM
Microbiology
74d
Cleared
Oct 25, 1988
FDL ELISA FOR CHLAMYDIA
Microbiology
83d
Cleared
Apr 27, 1988
BREWER GEL FOR CAMPYLOBACTER
Microbiology
16d
Cleared
Jan 27, 1988
BREWER GEL FOR ANAEROBES
Microbiology
27d
Cleared
Dec 23, 1985
DIRECT ELISA FOR HERPES SIMPLEX VIRUS
Microbiology
138d
Cleared
Feb 28, 1985
ROTALOK SURGICAL HAND TABLE
General & Plastic Surgery
37d