FDA 510(k) Applications Submitted by SERIM RESEARCH CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K992341	07/13/1999	CIDEX OPA SOLUTION TEST STRIP	SERIM RESEARCH CORP.
K012115	07/06/2001	SERIM BLOOD LEAK TEST STRIP-2	SERIM RESEARCH CORP.
K120652	03/02/2012	RAPICIDE OPA-28 TEST STRIP	SERIM RESEARCH CORP.
K080712	03/13/2008	SERIM HISENSE ULTRA 0.1, PART NUMBER 5167	SERIM RESEARCH CORP.
K081370	05/15/2008	SERIM DISINTEK OPA TEST STRIP	SERIM RESEARCH CORP.
K092346	08/04/2009	SERIM D-CIDE GTA 1.5% TEST STRIP, MODEL PART NUMBER 5171	SERIM RESEARCH CORP.
K083295	11/10/2008	SERIM DISINTEK GTA 2.1%, MODEL: 5164	SERIM RESEARCH CORP.
K014038	12/07/2001	PYLORITEK VP TEST KIT 5140VP	SERIM RESEARCH CORP.
K082352	08/16/2008	SERIM DISINTEK OPA TEST STRIP	SERIM RESEARCH CORP.
K052388	08/31/2005	SERIM PERACETIC ACID CHEMICAL INDICATOR	SERIM RESEARCH CORP.
K043031	11/03/2004	SERIM DIALYSATE MONITOR TEST STRIP	SERIM RESEARCH CORP.
K972035	06/02/1997	SPOROX TEST STRIPS	SERIM RESEARCH CORP.
K990206	01/21/1999	SERIM BLOOD LEAK TEST STRIP	SERIM RESEARCH CORP.
K000578	02/22/2000	SERIM LEUKOCYTE ESTERASE TEST STRIPS	SERIM RESEARCH CORP.