Dupont Medical Products - FDA 510(k) Cleared Devices
28
Total
28
Cleared
0
Denied
Dupont Medical Products has 28 FDA 510(k) cleared medical devices. Based in Wilmington, US.
Historical record: 28 cleared submissions from 1991 to 1995. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Dupont Medical Products Filter by specialty or product code using the sidebar.
28 devices
Cleared
Aug 31, 1995
DUPONT LIPASE CALIBRATOR
Chemistry
72d
Cleared
Aug 11, 1995
DUPONT DIMENSION TOTAL PROTEIN METHOD
Chemistry
163d
Cleared
Jul 20, 1995
LIPASE FLEX REAGENT CARTRIDGE
Chemistry
30d
Cleared
Jun 23, 1995
DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL
Toxicology
31d
Cleared
Mar 09, 1995
DUPONT DIMENSION C-REACTIVE PROTEIN METHOD
Immunology
132d
Cleared
Dec 28, 1994
PHENOBARBITAL FLEX REAGENT CARTRIDGE
Toxicology
83d
Cleared
Nov 10, 1994
DUPONT ACA STAR
Chemistry
248d
Cleared
Oct 20, 1994
DUPONT ACA PLUS LUTEINIZING HORMONE (LH) METHOD
Toxicology
65d
Cleared
Oct 03, 1994
DUPONT ACA PLUS THYROID STIMULATING HORMONE SYSTEM
Chemistry
207d
Cleared
Sep 09, 1994
DUPONT DIMENSION AMYLASE METHOD
Chemistry
98d
Cleared
Aug 18, 1994
DUPONT APC BLOOD COLLECTION CONTAINER WITH THROMBOPLASTIN
Chemistry
101d
Cleared
Aug 17, 1994
DUPONT APC BLOOD COLLECTION CONTAINER WITH LITHIUM HEPARIN
Chemistry
100d