The DU Pont Co.
The DU Pont Co. appears in FDA public data with 0 recalls, 13 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 7, 1995.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 13
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K953475 | CDS COMPACT DAYLIGHT CASSETTE FOR VIDEO IMAGING | October 7, 1995 |
| K953477 | MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING | October 7, 1995 |
| K952891 | CRONEX LOW ABSORPTION CASSETTE | July 13, 1995 |
| K945125 | DUPONT ACA VANCOMYCIN (VANC) METHOD | March 10, 1995 |
| K943704 | LIPASE CALIBRATOR | September 14, 1994 |
| K900492 | LABELING CHANGE - VIASPAN(TM) (BELZER UW) | March 20, 1990 |
| K885259 | ACA THYRONINE UPTAKE (TU E) METHOD | February 17, 1989 |
| K885258 | ACA THYROXINE (T4 E) METHOD | February 17, 1989 |
| K884700 | ANALYST THYROXINE (T4) ROTOR | January 27, 1989 |
| K884169 | DU PONT ANALYST THYROID ROTOR | January 24, 1989 |
| K884168 | ANALYST THYROXINE (T4) & THYRONINE UPTAKE CALIBRA. | November 29, 1988 |
| K884170 | ANALYST THEOPHYLLINE CALIBRATOR | November 16, 1988 |
| K884002 | ANALYST THEOPHYLLINE ROTOR | October 31, 1988 |