FDA 510(k) Applications Submitted by BRIAN SCHLIESMAN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K030687	03/05/2003	K-ASSAY D-DIMER, K-ASSAY D-DIMER CALIBRATOR, MODELS KAI-090; KAJ-091C	KAMIYA BIOMEDICAL CO.
K050944	04/14/2005	K-ASSAY FERRITIN (2) & FERRITIN CALIBRATOR SET	KAMIYA BIOMEDICAL CO.
K021660	05/20/2002	K-ASSAY LP(A) ASSAY	KAMIYA BIOMEDICAL CO.
K022486	07/29/2002	K-ASSAY HS-CRP CONTROLS	KAMIYA BIOMEDICAL CO.
K042241	08/19/2004	K-ASSAY TOTAL IGE, K-ASSAY IGE CALIBRATOR SET, MODELS KAI-092/KAI-093C	KAMIYA BIOMEDICAL CO.
K023828	11/18/2002	K-ASSAY C-REACTIVE PROTEIN (3), K-ASSAY CRP MULTI-CALIBRATOR D, K-ASSAY CRP MULTI-CALIBRATOR E, K-ASSAY CRP MULTI-CALIBR	KAMIYA BIOMEDICAL CO.
K023853	11/19/2002	K-ASSAY LP(A) CONTROLS	KAMIYA BIOMEDICAL CO.