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 |