Company ยท US
The DU Pont Co.
FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1995. Name variants (Inc, Corp, punctuation) are merged.
13510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| KLI | Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine | 2 |
| LMC | Camera, Multi Format, Radiological | 2 |
| CEL | Ammonium Molybdate And Ammonium Vanadate, Phospholipids | 1 |
| DLJ | Calibrators, Drug Specific | 1 |
| IXA | Cassette, Radiographic Film | 1 |
| JIS | Calibrator, Primary | 1 |
| JIT | Calibrator, Secondary | 1 |
| KDL | Set, Perfusion, Kidney, Disposable | 1 |
| KHQ | Radioassay, Triiodothyronine Uptake | 1 |
| KLS | Enzyme Immunoassay, Theophylline | 1 |
| LEH | Radioimmunoassay, Vancomycin | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 7, 1995 | K953477 | MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING The DU Pont Co. | LMC |
| Oct 7, 1995 | K953475 | CDS COMPACT DAYLIGHT CASSETTE FOR VIDEO IMAGING The DU Pont Co. | LMC |
| Jul 13, 1995 | K952891 | CRONEX LOW ABSORPTION CASSETTE The DU Pont Co. | IXA |
| Mar 10, 1995 | K945125 | DUPONT ACA VANCOMYCIN (VANC) METHOD The DU Pont Co. | LEH |
| Sep 14, 1994 | K943704 | LIPASE CALIBRATOR The DU Pont Co. | JIT |
| Mar 20, 1990 | K900492 | LABELING CHANGE - VIASPAN(TM) (BELZER UW) The DU Pont Co. | KDL |
| Feb 17, 1989 | K885259 | ACA THYRONINE UPTAKE (TU E) METHOD The DU Pont Co. | KHQ |
| Feb 17, 1989 | K885258 | ACA THYROXINE (T4 E) METHOD The DU Pont Co. | KLI |
| Jan 27, 1989 | K884700 | ANALYST THYROXINE (T4) ROTOR The DU Pont Co. | KLI |
| Jan 24, 1989 | K884169 | DU PONT ANALYST THYROID ROTOR The DU Pont Co. | CEL |
| Nov 29, 1988 | K884168 | ANALYST THYROXINE (T4) & THYRONINE UPTAKE CALIBRA. The DU Pont Co. | JIS |
| Nov 16, 1988 | K884170 | ANALYST THEOPHYLLINE CALIBRATOR The DU Pont Co. | DLJ |
| Oct 31, 1988 | K884002 | ANALYST THEOPHYLLINE ROTOR The DU Pont Co. | KLS |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||