The DU Pont Co.
The DU Pont Co. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1995.
Top product codes for The DU Pont Co.
Recent clearances by The DU Pont Co.
- K953475 — CDS COMPACT DAYLIGHT CASSETTE FOR VIDEO IMAGING
- K953477 — MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING
- K952891 — CRONEX LOW ABSORPTION CASSETTE
- K945125 — DUPONT ACA VANCOMYCIN (VANC) METHOD
- K943704 — LIPASE CALIBRATOR
- K900492 — LABELING CHANGE - VIASPAN(TM) (BELZER UW)
- K885258 — ACA THYROXINE (T4 E) METHOD
- K885259 — ACA THYRONINE UPTAKE (TU E) METHOD
- K884700 — ANALYST THYROXINE (T4) ROTOR
- K884169 — DU PONT ANALYST THYROID ROTOR
- K884168 — ANALYST THYROXINE (T4) & THYRONINE UPTAKE CALIBRA.
- K884170 — ANALYST THEOPHYLLINE CALIBRATOR
- K884002 — ANALYST THEOPHYLLINE ROTOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.