FDA 510(k) Applications Submitted by CATHY P CRAFT

FDA 510(k) Number Submission Date Device Name Applicant
K011852 06/12/2001 DIMENSION HAIC ASSAY, MODEL DF105 DADE BEHRING, INC.
K990251 01/27/1999 DGTX FLEX REAGENT CARTRIDGE, MODEL DF36 DADE BEHRING, INC.
K990255 01/27/1999 DIMENSION DRUG CALIBRATOR II, MODEL DC49B DADE BEHRING, INC.
K970336 01/29/1997 MMB CALIBRATOR DADE CHEMISTRY SYSTEMS, INC.
K970343 01/29/1997 MMB METHOD DADE CHEMISTRY SYSTEMS, INC.
K970389 02/03/1997 THYROID CALIBRATOR DADE CHEMISTRY SYSTEMS, INC.
K990551 02/22/1999 IGG FLEX REAGENT CARTRIDGE DADE BEHRING, INC.
K990552 02/22/1999 IMMUNOGLOBULIN A TEST SYSTEM DADE BEHRING, INC.
K990553 02/22/1999 IGM FLEX REAGENT CARTRIDGE DADE BEHRING, INC.
K990554 02/22/1999 DIMENSION SPECIAL PROTEIN CALIBRATOR DADE BEHRING, INC.
K971141 03/28/1997 FT4 METHOD FOR THE DIMENSION RXL CLINICAL CHEMISTRY SYSTEM DADE CHEMISTRY SYSTEMS, INC.
K962594 07/02/1996 ACA PLUS FT4 CALIBRATOR DADE INTL., INC.
K962602 07/02/1996 ACA PLUS FREE THYROXINE(FT4) METHOD DADE INTL., INC.
K963493 09/03/1996 FERRITIN CALIBRATOR DADE CHEMISTRY SYSTEMS, INC.
K963498 09/03/1996 FERR FLEX REAGENT CARTRIDGE DADE CHEMISTRY SYSTEMS, INC.
K983548 10/09/1998 FERRITIN CALIBRATOR DADE BEHRING, INC.
K003209 10/13/2000 URINE OPIATES (OPI) SCREEN FLEX REAGENT CARTRIDGE, CATALOG NO. DF93A DADE BEHRING, INC.


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