FDA 510(k) Applications for Medical Device Product Code "DII"
(Columns, Glc)

FDA 510(k) Number Applicant Device Name Decision Date
K791893 HEWLETT-PACKARD CO. 19091-XXXXX SER. OF GLASS CAPILLARY COL. 10/30/1979
K844164 LKB INSTRUMENTS, INC. REACTIFS, IBF ULTROGELS ACA & ULTROGELS A 12/10/1984
K862542 SUPELCO, INC. CAPILLARY COLUMNS FOR GAS CHROMATOGRAPHY 08/04/1986
K874824 SUPELCO, INC. CAPILLARY COLUMNS FOR GAS CHROMATOGRAPHY 01/21/1988
K841712 SUPELCO, INC. CAPILLARY GAS CHROMATOGRAPHIC COLUMNS 05/21/1984


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