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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