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Dupont Medical Products

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
28
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K952815DUPONT LIPASE CALIBRATORAugust 31, 1995
K950920DUPONT DIMENSION TOTAL PROTEIN METHODAugust 11, 1995
K952816LIPASE FLEX REAGENT CARTRIDGEJuly 20, 1995
K952412DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROLJune 23, 1995
K945280DUPONT DIMENSION C-REACTIVE PROTEIN METHODMarch 9, 1995
K944932PHENOBARBITAL FLEX REAGENT CARTRIDGEDecember 28, 1994
K941050DUPONT ACA STARNovember 10, 1994
K943996DUPONT ACA PLUS LUTEINIZING HORMONE (LH) METHODOctober 20, 1994
K941146DUPONT ACA PLUS THYROID STIMULATING HORMONE SYSTEMOctober 3, 1994
K942640DUPONT DIMENSION AMYLASE METHODSeptember 9, 1994
K942241DUPONT APC BLOOD COLLECTION CONTAINER WITH THROMBOPLASTINAugust 18, 1994
K942240DUPONT APC BLOOD COLLECTION CONTAINER WITH LITHIUM HEPARINAugust 17, 1994
K941219DUPONT ACA PLUS FSH/LH/PROLACTIN CALIBRATORAugust 9, 1994
K943024KINASE ISOENZYMEAugust 2, 1994
K941221DUPONT ACA PLUS IMMUNOASSAY SYSTEM FOLLICLE STIMULATING HORMONEJuly 20, 1994
K941475CRONEX REGULAR CASSETTEJuly 20, 1994
K941584CREATINE KINASE METHODJuly 6, 1994
K941518DUPONT CRONEX PORTABLE GRID CASSETTEJune 6, 1994
K941220DUPONT ACA PLUS PROLACTIN (PROL) METHODJune 3, 1994
K936202URINARY ALBUMIN TEST PACKMay 9, 1994