Denley Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Denley Instruments, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Denley Instruments, Inc. has 9 FDA 510(k) cleared medical devices. Based in Durham, US.
Historical record: 9 cleared submissions from 1989 to 1992. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Denley Instruments, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Denley Instruments, Inc.
9 devices
Cleared
Nov 05, 1992
WELLWASH 4 MARK II
Chemistry
148d
Cleared
Aug 12, 1992
DENLEY WELLPREP 2 SAMPLE PROCESSOR
Hematology
93d
Cleared
Aug 11, 1992
WELLPREP 2000 SAMPLE PROCESSOR
Chemistry
92d
Cleared
Jan 22, 1992
STACKING MICROPLATE WASHER
Chemistry
58d
Cleared
Oct 04, 1991
WELLPREP 1
Chemistry
56d
Cleared
May 17, 1990
MICROPLATE REAGENT DISPENSER
Chemistry
98d
Cleared
Aug 21, 1989
DENLEY ANTHOS 2001 READER
Chemistry
60d
Cleared
Aug 21, 1989
DENLEY WELLDILL 3
Chemistry
60d
Cleared
Aug 15, 1989
DENLEY WELLWASH 2 AND 4
Chemistry
54d