The DU Pont Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K953477MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGINGOctober 7, 1995
K953475CDS COMPACT DAYLIGHT CASSETTE FOR VIDEO IMAGINGOctober 7, 1995
K952891CRONEX LOW ABSORPTION CASSETTEJuly 13, 1995
K945125DUPONT ACA VANCOMYCIN (VANC) METHODMarch 10, 1995
K943704LIPASE CALIBRATORSeptember 14, 1994
K900492LABELING CHANGE - VIASPAN(TM) (BELZER UW)March 20, 1990
K885258ACA THYROXINE (T4 E) METHODFebruary 17, 1989
K885259ACA THYRONINE UPTAKE (TU E) METHODFebruary 17, 1989
K884700ANALYST THYROXINE (T4) ROTORJanuary 27, 1989
K884169DU PONT ANALYST THYROID ROTORJanuary 24, 1989
K884168ANALYST THYROXINE (T4) & THYRONINE UPTAKE CALIBRA.November 29, 1988
K884170ANALYST THEOPHYLLINE CALIBRATORNovember 16, 1988
K884002ANALYST THEOPHYLLINE ROTOROctober 31, 1988