FDA 510(k) Applications Submitted by MARY REES

FDA 510(k) Number Submission Date Device Name Applicant
K971985 05/29/1997 N-ASSAY TIA PLASMINOGEN TEST KIT CRESTAT DIAGNOSTICS, INC.
K972257 06/17/1997 N-ASSAY TIA ANTITHROMBIN III TEST KIT CRESTAT DIAGNOSTICS, INC.
K933970 08/13/1993 N-ASSAY TIA IGM CRESTAT DIAGNOSTICS, INC.
K933971 08/13/1993 N-ASSAY TIA IGA CRESTAT DIAGNOSTICS, INC.
K933972 08/13/1993 N-ASSAY TIA IGG CRESTAT DIAGNOSTICS, INC.
K933973 08/13/1993 N-ASSAY TIA MULTI V-NL CRESTAT DIAGNOSTICS, INC.
K934143 08/24/1993 N-ASSAY TIA MICROALBUMIN CALIBRATOR SET CRESTAT DIAGNOSTICS, INC.
K934146 08/24/1993 N-ASSAY TIA MICROALBUMIN CRESTAT DIAGNOSTICS, INC.
K964415 10/01/1996 N-ASSAY TIA RHEUMATOID FACTOR TEST KIT KAMIYA TECHNOLOGY SERVICES
K964418 10/01/1996 N-ASSAY TIA RHEUMATOID FACOTR MULTI-CALIBRATOR SET KAMIYA TECHNOLOGY SERVICES
K965024 12/17/1996 N-ASSAY TIA C1-INACTIVATOR TEST KIT CRESTAT DIAGNOSTICS, INC.
K965100 12/20/1996 N-ASSAY TIA ALPHA-1-ANTITRYPSIN TEST KIT CRESTAT DIAGNOSTICS, INC.
K965110 12/20/1996 N-ASSAY TIA MULTI CRP CALIBRATOR SET CRESTAT DIAGNOSTICS, INC.
K965113 12/20/1996 N-ASSAY TIA FIBRINOGEN TEST KIT CRESTAT DIAGNOSTICS, INC.
K905829 12/31/1990 DETERMINER PL/DETERMINATION OF PHOSPHOLIPIDS KAMIYA BIOMEDICAL CO.


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