FDA 510(k) Applications for Medical Device Product Code "DJY"
(Ion-Exchange Chromatography)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K800061 | ANALYTICHEM INTERNATIONAL, INC. | BOND ELUT COLUMNS | 03/12/1980 |
| K831289 | BERWICK MEDICAL PRODUCTS, INC. | PREFILLED IEC COLUMNS | 06/16/1983 |
| K890113 | CARDIOVASCULAR DEVICES, INC. | THE CDI(R) SYSTEM 400 | 05/23/1989 |
| K830692 | E.I. DUPONT DE NEMOURS & CO., INC. | DUPONT PREP OD EXTRACTION CARTRIDE | 04/05/1983 |
| K830693 | E.I. DUPONT DE NEMOURS & CO., INC. | DUPONT PREP TYPE AS EXTRACTION CARTRIDE | 04/05/1983 |
| K850963 | E.I. DUPONT DE NEMOURS & CO., INC. | DUPONT PREP TYPE SI EXTRACITON CARTRIDGE | 03/25/1985 |
| K823697 | E.I. DUPONT DE NEMOURS & CO., INC. | PREP TYPE A EXTRACTION CARTRIDGE | 01/05/1983 |
| K832198 | HAMILTON CO. | HC40/HC75 PREPACKED COLUMS | 08/12/1983 |
| K840985 | LKB INSTRUMENTS, INC. | TRISACRYL GF 05 & TRISACRYL GF 2000 | 04/19/1984 |
| K883615 | SUPELCO, INC. | LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/73 | 12/16/1988 |
| K881361 | SUPELCO, INC. | SOLID PHASE EXTRACTION TUBES | 08/08/1988 |
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