Dupont Medical Products
Dupont Medical Products holds FDA 510(k) medical device clearances, first cleared 1991, most recent 1995.
Top product codes for Dupont Medical Products
Recent clearances by Dupont Medical Products
- K952815 — DUPONT LIPASE CALIBRATOR
- K950920 — DUPONT DIMENSION TOTAL PROTEIN METHOD
- K952816 — LIPASE FLEX REAGENT CARTRIDGE
- K952412 — DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL
- K945280 — DUPONT DIMENSION C-REACTIVE PROTEIN METHOD
- K944932 — PHENOBARBITAL FLEX REAGENT CARTRIDGE
- K941050 — DUPONT ACA STAR
- K943996 — DUPONT ACA PLUS LUTEINIZING HORMONE (LH) METHOD
- K941146 — DUPONT ACA PLUS THYROID STIMULATING HORMONE SYSTEM
- K942640 — DUPONT DIMENSION AMYLASE METHOD
- K942241 — DUPONT APC BLOOD COLLECTION CONTAINER WITH THROMBOPLASTIN
- K942240 — DUPONT APC BLOOD COLLECTION CONTAINER WITH LITHIUM HEPARIN
- K941219 — DUPONT ACA PLUS FSH/LH/PROLACTIN CALIBRATOR
- K943024 — KINASE ISOENZYME
- K941221 — DUPONT ACA PLUS IMMUNOASSAY SYSTEM FOLLICLE STIMULATING HORMONE
- K941475 — CRONEX REGULAR CASSETTE
- K941584 — CREATINE KINASE METHOD
- K941518 — DUPONT CRONEX PORTABLE GRID CASSETTE
- K941220 — DUPONT ACA PLUS PROLACTIN (PROL) METHOD
- K936202 — URINARY ALBUMIN TEST PACK
- K936201 — URINARY ALBUMIN CALIBRATOR
- K932732 — ACA(R) DIGOXIN ANALYTICAL TEST PACK (DGN)
- K933161 — ULTRA-VISION SUPER RAPID INTENSIFYING SCREEN
- K933648 — ADDED USE CLAIM FOR DUPONT ACA BETA-2-MICROGLOBULIN TEST PACK
- K930501 — DU PONT ACA NEV/EEV VERIFIER
- K932044 — DU PONT ISE SENSOR CARTRIDGE/REVISED TCO2 ELECTROD
- K915106 — DIMENSION AR CLINICAL CHEMISTRY SYSTEM
- K910354 — DU PONT IDENTIFICATION CAMERA
Data sourced from openFDA. This site is unofficial and independent of the FDA.